7001 to 8000 most common queries

List represents a sample of symptoms, diseases, and other queries. Updated weekly.

• Wedge Defect of Tooth
• Absolute Glaucoma
• Bowenoid Papulosis
• Irons-Bhan Syndrome
• Oropharyngeal Carcinoma
• Davis-Lafer Syndrome
• Partial Trisomy 18q
• Low T3 Syndrome
• Pathophobia
• Macular Cutaneous Amyloidosis
• Cannabis Withdrawal
• Trifoliate Orange Poisoning
• Genital Psoriasis
• Rowley-Rosenberg Syndrome
• Trichosporon
• Inflammatory Bowel Disease Type 6
• Steroid Abuse
• Schizophrenia Type 11
• Aase Syndrome
• Allodynia
• Tonsillar-Pharyngeal Diphteria
• Angioma of the Lip
• Noctiphobia
• Hyperemia
• Palant Cleft Palate Syndrome
• Hypnic Jerk
• Borries Syndrome
• Periventricular Laminar Heterotopia
• Wallerian Degeneration
• Follicular Large-Cell Lymphoma
• Sakamoto Disease
• Zephyranthes Atamasco Poisoning
• Hereditary Spherocytosis Type 2
• Thomas-Jewett-Raines Syndrome
• Chondritis
• Acute Stress Disorder
• Akaba-Hayasaka Syndrome
• Phorate Poisoning
• Roseola Infantum
• Submandibular Gland Adenocarcinoma
• Bernheim Syndrome
• Chondromatosis
• Plica Syndrome
• Drug-Induced Sideroblastic Anemia
• Wisconsin Syndrome
• Local Anaesthetic Allergy
• Inflammatory Bowel Disease Type 9
• Staphylococcal Toxic Shock Syndrome
• Acute Hepatitis B
• Insect Allergy
• Hyperosmolar Hyperglycemic Non-Ketotic Syndrome
• Molybdenum Deficiency
• Type A Influenza Subtype H1N2
• Inflammatory Bowel Disease Type 10
• Taijin-Kyofusho Syndrome
• Hyperandrogenism
• Acute Lymphoblastic Leukemia Type L1
• Intervertebral Disc Disease
• Silent Myocardial Infarction
• Mumps-Associated Pancreatitis
• Cone Shell Poisoning
• Navajo Poikiloderma
• Hypertrophic Subaortic Stenosis
• Macrocytic Hyperchromic Anemia
• Susceptibility to Celiac Disease 9
• Schizotypal Personality Disorder
• Goldstein-Hutt Syndrome
• Ramsay-Hunt Cerebellar Syndrome
• Laryngitis
• Jatropha Multifida Poisoning
• Mirizzi Syndrome
• Isospora Belli Infection
• Susceptibility to Celiac Disease 6
• Pseudoinflammatory Fundus Dystrophy
• Alveolar Periostitis
• Autoimmune Disease of the Nervous System
• Oral Squamous Cell Carcinoma Stage 4
• Atypical Rett Syndrome
• Respiratory Sounds
• Pointer Syndrome
• Acephalgic Migraine
• Ziprkowski-Margolis Syndrome
• Nasal-Type Extranodal NK-T-Cell Lymphoma Stage 3
• Space Adaptation Syndrome
• Infantile Apnea
• Adrenal Hypertension
• Congenital Symmetric Circumferential Skin Creases Type 1
• Acute Hepatitis D
• Excoriated Acne
• Chronic Pharyngitis
• Macrognathism
• Laurence-Prosser-Rocker Syndrome
• Opium Addiction
• Acute Hepatitis A
• Vascular Malformations of the Brain
• Vitamin C Deficiency
• Submandibular Gland Carcinoma
• Traumatic Laryngitis
• Nodular Scleritis
• Globulomaxillary Cyst
• Aspergillus Niger Infection
• Burnett-Schwartz-Berberian Syndrome
• Complex Migraine
• Trisomy 3
• Large Cell Carcinoma
• Hereditary Sensory and Autonomic Neuropathy Type 2
• Mansonella Ozzardi Infection
• Dipylidiasis
• Mosaic Trisomy 17
• Shwartzman Phenomenon
• Accessory Navicular Bone
• Tang Hsi Ryu Syndrome
• Hypopharyngeal Tumor
• Benign Oral Neoplasm
• Glassy Cell Carcinoma of the Cervix
• Heroin Overdose
• Lantana Poisoning
• Jeune-Tommasi Syndrome
• Partial Trisomy 10q
• Faye-Petersen-Ward-Carey Syndrome
• Acute Hepatitis E
• Contact Dermatitis due to Drugs
• Catarrh
• Ecstasy Overdose
• Primary Insomnia
• Angioma
• Ameloblastic Fibroma
• Bowel Bypass Syndrome
• Bronze Baby Syndrome
• Gullner Syndrome
• Herpes Simplex Keratitis
• Camera-Marugo-Cohen Syndrome
• Aquired Fibrokeratoma
• Iliohypogastric Nerve Disorder
• Notalgia Paresthetica
• Adenocarcinoid Tumor
• Lateral Periodontal Cyst
• Rectal Abscess
• Posthemorrhagic Hydrocephalus
• Cutaneous Necrotizing Vasculitis
• Methylene Chloride - Occupational Liver Damage
• Acute Congestive Hepatopathy
• Cherry Laurel Poisoning
• Spinal Dural Arteriovenous Fistula
• Trisomy 13q
• Fistula
• Blegvad-Haxthausen Syndrome
• Follicular Cyst
• Anorectal Atresia
• Ectopic Acromegaly
• Pyrrolizidine Alkaloids Poisoning
• Schizophrenia Type 5
• Invasive Breast Cancer
• Partial Monosomy 11q
• Pulmonary Sarcoidosis Type 3
• Corneal Endothelial Dystrophy Type 1
• Senile Retinoschisis
• Familial Paget Disease of Bone
• Genitofemoral Nerve Disorder
• Colonic Inertia
• Autophobia
• Intestinal Duplication
• Leg Injury
• Inflammatory Bowel Disease Type 21
• Fungal Infection of Hair
• Silicosiderosis
• Benign Tongue Neoplasm
• Shaken Baby Syndrome
• Coral Bean Poisoning
• Toxic Pulmonary Edema
• Exercise-Induced Asthma
• Pancoast Tumor
• Erythroderma Desquamativa of Leiner
• Lymphatic Obstruction
• Immunoproliferative Diseases
• Hyperoxia
• Tulip Poisoning
• Kasznica-Carlson-Coppedge Syndrome
• Cardiogenic Pulmonary Edema
• Marijuana Addiction
• Kuster Syndrome
• Ovarian Remnant Syndrome
• Neurasthenia
• Nephritic Syndrome
• Chronic Ulcerative Pulpitis
• Digital Flexor Tendon Rupture
• Borderline Personality Disorder
• Lidocain Poisoning
• Oral Squamous Cell Carcinoma
• Pharmacophobia
• Finger Arthritis
• Dieterich's Disease
• Chromosome 6q Duplication Syndrome
• Bacterial Pericarditis
• TAU Syndrome
• Bartter Syndrome Type 4
• Maple Syrup Urine Disease Type 2
• Chlorodontia
• Oculo-Oto-Facial Dysplasia
• Lymphatic System Tumors
• Repetitive Strain Injury
• Darvocet Withdrawal
• Trueb-Burg-Bottani Syndrome
• Acute Hepatitis C
• Telencephalic Leukoencephalopathy
• Childhood Hodgkin Lymphoma
• Hemorrhoids Grade 4
• Benign Multiple Sclerosis
• Acute Viral Bronchiolitis
• Anterior Interosseous Nerve Disorder
• Actinic Cheilitis
• Myopia Type 2
• Selective Mutism
• Flea-Borne Infectious Diseases
• Cat Allergy
• Post-Traumatic Epilepsy
• Pseudoainhum
• Partial Monosomy 13q
• Agyrophobia
• Thirst Fever
• Hooft Disease
• Multicentric Reticulohistiocytosis
• Scapulocostal Syndrome
• Partial Trisomy 15q
• Calculi
• Infantile Gluteal Granuloma
• Partial Trisomy 9p
• Disulfiram Poisoning
• Nodular Sclerosing Classical Hodgkin Lymphoma
• Toe Arthritis
• Asymmetric Short Stature Syndrome
• Palate Cancer
• Monosomy 2q
• Brainstem Auditory Evoked Responses
• Connatal Pelizaeus-Merzbacher Disease
• Cold Skin
• Descending Perineum Syndrome
• Amaurosis Fugax
• Zinc Poisoning
• Megalocytic Interstitial Nephritis
• Type A Influenza Subtype H9N2
• Narcolepsy without Cataplexy
• Ameloblastic Fibro-Odontosarcoma
• Cathinone Poisoning
• Glycoprotein Storage Disease
• Selig-Benacerraf-Greene Syndrome
• Microspherophakia with Hernia
• Eastern Brown Snake Poisoning
• Connective Tissue Nevus
• Bing-Neel Syndrome
• Essential Thrombocytopenia
• May-White Syndrome
• Arcobacter Cryaerophilus Infection
• Kappa Light Chain Myeloma
• Anisometropia
• Myopathic Carnitine Deficiency
• Acquired Hypothyroidism
• Eosinophilic Synovitis
• Hepatic Jaundice
• Aflatoxin B1
• Karandikar-Maria-Kamble Syndrome
• Acquired Lactase Deficiency
• Wandering Spleen
• Amlodipine
• Fournier Gangrene
• Berlin Syndrome
• Microphobia
• Devriendt Syndrome
• Intraventricular Hemorrhage of the Premature Infant
• Hypervitaminosis B Complex
• Familial Hypertrophic Cardiomyopathy Type 3
• Trichloroethane - Kidney Damage
• Iris Hypoplasia and Glaucoma
• Copper Poisoning
• 2p12-p11.2 Deletion Syndrome
• Berk-Tabatznik Syndrome
• Le Marec-Bracq-Picaud Syndrome
• Lattice Corneal Dystrophy Type 2
• Suppurative Parotitis
• Inflammatory Bowel Disease Type 20
• Odontogenic Carcinosarcoma
• Ameloblastic Fibro-Odontoma
• Cardiac Sarcoidosis
• Charcot-Marie-Tooth Disease Type 2A
• Iida-Kannari Syndrome
• Odontophobia
• Phacolytic Glaucoma
• Abalone Poisoning
• Phyllodes Tumor of the Prostate
• Muller-Barth-Menger Syndrome
• Duplication of Whole Lower Limb
• Dehydratase Deficiency
• Babinski-Nageotte Syndrome
• Cervicogenic Headache
• Mansonella Perstans Infection
• Perianal Thrombosis
• Steroid Rosacea
• Quinolone - Drug-Induced Liver Damage
• Infection with Oesophagostomum Spp.
• Pudendal Nerve Entrapment
• Boron Deficiency
• Abdominal Neoplasm
• Tabatznik Syndrome
• Acute Sphenoidal Sinusitis
• Lupus Nephritis WHO Class 2
• Eosinophilic Meningitis
• Dysmorphophobia
• Hexane - Chemical Poisoning
• Abnormal Body Odor
• Ossifying Fibroma
• Malignant Tongue Neoplasm
• Olfactory Nerve Disorder
• Sublingual Gland Neoplasm
• Erotophobia
• Mosquito Bite
• Visual Pathway Glioma
• Siderosis
• Primary Autoimmune Hemolytic Anemia
• Non-Scarring Alopecia
• Potato Nose
• Primary Intraosseous Carcinoma
• Trisomy 15q
• Postmenopausal Osteoporosis
• Colonic Volvulus
• Primary Biliary Cirrhosis 1
• Catarrhal Otitis Media
• Allen-Masters Syndrome
• Nodular Malignant Melanoma
• Superficial Spreading Melanoma
• Limb-Body Wall Complex
• Lung Fibroma
• Osteochondrosis
• Astley-Kendall Syndrome
• Hyperkinetic Dysarthria
• Malignant Eye Neoplasm
• Transient Osteoporosis of the Hip
• Human T-Lymphotropic Virus Type 3
• X-linked Mental Retardation Type 12
• Susceptibility to Celiac Disease 7
• Infectious Diarrhea
• Submandibular Gland Acinic Cell Carcinoma
• Battaglia-Neri Syndrome
• Littoral Cell Angioma of the Spleen
• Tonic Seizure
• Seghers Syndrome
• Multiple Myeloma Type IgD
• Parotid Gland Warthin Tumor
• Arterial Priapism
• Nasal Tuberculosis
• FG Syndrome Type 2
• Rape Trauma Syndrome
• Charcot-Marie-Tooth Disease with Deafness - Mental Retardation - Absence of Large Myelinated Fibers
• Adult Myxedema
• Early-Onset Nemaline Myopathy
• Louse-Borne Diseases
• Jaffer-Beighton Syndrome
• Naphthalene
• Benadryl -- Teratogenic Agent
• Variant Creutzfeldt-Jakob Disease
• Gastric Erosion
• Partial Trisomy 3q
• Inflammatory Bowel Disease Type 15
• Autoimmune Progesterone Dermatitis
• Brachioskeletogenital Syndrome
• Autosomal Dominant Polycystic Kidney Disease Type 2
• Chronic Venous Insufficiency 
• Zoophobia
• Parathyroid Hyperplasia
• Physical Addiction
• Paramolar
• Factor XIII Deficiency
• Colorectal Polyps
• Atheroma
• Dissociated Sensory Loss
• Coitophobia
• Adenitis
• Ventricular Flutter
• Monosomy 3p
• Tuberculous Uveitis
• Malignant Penile Neoplasm
• Sarcomatoid Mesothelioma
• Amelogenesis Imperfecta Hypoplastic Type
• Nutritional Anemia
• Haptophobia
• Crumpled Helices and Small Mouth
• Scapuloperoneal Myopathy
• Dibasic Aminoaciduria Type 1
• Abdominal Cystic Lymphangioma
• Meningioma 1
• Secondary Insomnia
• Hodgkin Lymphoma during Pregnancy
• Piperazine -- Teratogenic Agent
• Trimethylaminuria
• Spermatophobia
• Primary Open-Angle Glaucoma Type 1B
• Death Camas Poisoning
• Primary Open-Angle Glaucoma Type 1I
• Granulomatous Cheilitis
• Schlegelberger-Grote Syndrome
• Cephalic Disorders
• Familial Hyperlipoproteinemia
• Visceral Pain
• Ulcerative Proctosigmoiditis
• Chronic Paroxysmal Hemicrania
• Bacterial Corneal Ulcer
• Hereditary Nephrotic Syndrome
• Blitz-Nick-Salaam Attacks
• Avascular Necrosis of Humerus
• Diphenoxylate -- Teratogenic Agent
• Trisomy 12p
• Valsartan -- Teratogenic Agent
• Infective Endocarditis
• Diffuse Neonatal Hemangiomatosis
• Elbow Injury
• Heliotrope Poisoning
• Bone and Cartilage Tumors
• Carbon Monoxide -- Teratogenic Agent
• Hypokinetic Dysarthria
• Gestational Diabetes
• Partial Monosomy 8q
• Pelvic Lipomatosis
• Hypodermyiasis
• Colorectal Carcinoma
• Avian Influenza
• Phototoxic Eczema
• SAPHO Syndrome
• Chromosome 7p Duplication Syndrome
• Twin-Twin Transfusion Syndrome
• Dilaudid
• Biliary Disorder
• Non-Allergic Asthma
• Posterior Tibial Tendon Rupture
• Squamous Cell Neoplasm
• Megaduodenum and/or Megacystis
• Amnesic Shellfish Poisoning
• Pulmonary Venous Hypertension
• Facial Parasthesia
• Spencer Disease
• Diverticulosis of the Ileum
• Hedblom Syndrome
• Psychological Dependence
• Bhaskar-Jagannathan Syndrome
• Lucio Phenomenon
• Juvenile Tay-Sachs Disease
• Phenol Sulfotransferase Deficiency
• Macular Hole
• Deep Scleritis
• Premature Aging Type Okamoto
• Königsmark-Knox-Hussels Syndrome
• Grasp Reflex
• Drug-Induced Headache
• Sea Urchin Poisoning
• Parotid Gland Carcinoma
• Sindbis Fever
• Partial Monosomy 21q
• Polyphobia
• FG Syndrome Type 3
• Ochlophobia
• Lymphoblastic Lymphoma
• Chronic Dacryocystitis
• Noise-Induced Hearing Loss
• Laryngopharyngeal Reflux
• Porcelain Gallbladder
• Hemolytic Jaundice
• Helicobacter Cinaedi Infection
• Perinatal Hypophosphatasia
• Tollner-Horst-Manzke Syndrome
• Palpebral Dermoid Cyst
• Jaw Conditions
• Isothiazolinone Allergy
• Sudden Arrhythmic Death Syndrome
• Arcobacter Butzleri Infection
• Hemochromatosis Type 2
• Parotid Gland Carcinosarcoma
• Upper Back Sprain
• Hereditary Factor VII Deficiency
• Pulsus Bisferiens
• Dorsiflexion Deformity of Foot
• Senna Obtusifolia Poisoning
• Sun Allergy
• Ribbing Disease
• Lentigo Maligna
• Monophobia
• Juvenile Scleroderma
• Glucose-Stimulated Secretory Diarrhea - Common Variable Immunodeficiency
• Uremic Pericarditis
• Trisomy 4 with or without Mosaicism
• Hecht Giant Cell Pneumonia in Measles
• Agenesis of Pulmonary Artery
• Paroxysmal Nocturnal Dyspnea
• Bertielliasis
• Kennerknecht Syndrome
• Autosomal Dominant Autoimmune Polyendocrine Syndrome Type 1
• Charcot-Marie-Tooth Disease Type 1 with Aplasia Cutis Congenita
• Hypoketonemic Hypoglycemia
• Achrestic Anemia
• MSI-H Colorectal Cancer
• Miliaria
• Hornova-Dlurosova Syndrome
• Brachydactyly Type A3
• Susceptibility to Celiac Disease 11
• Loquat Poisoning
• Rheumatoid Vasculitis
• Neuroma
• Smoldering Adult T-Cell Leukemia
• Meigel Disease
• Imerslund-Gräsbeck Syndrome
• Skunk Cabbage Poisoning
• AIDS-Related Opportunistic Infections
• Panophthalmitis
• Acute Arterial Occlusion
• Rhinolith
• Cardiac Compression Syndrome
• Cramp-Fasciculations Syndrome
• Ballantyne-Runge Syndrome
• Trisomy 22q11-q13
• Chromosome 1q Duplication Syndrome
• Bathophobia
• Chromosome 12p Deletion Syndrome
• Roy-Maroteaux-Kremp Syndrome
• Optic Nerve Sheath Meningioma
• Allergenic Cross-Reactivity
• Combined Small-Cell Carcinoma
• Philadelphia Chromosome Negative Chronic Myeloid Leukemia
• Respiratory Arrest
• Cherry Laurel Seed Poisoning
• Gynophobia
• Pyorrhea
• Funiculitis
• Dental Disorder
• Atropa Belladonna
• Mechanical Complication of Prosthetic Joint
• Primary Progressive Multiple Sclerosis
• Carpal Instability
• Ligament Tear
• Rectal Ulceration
• Internal Joint Prosthesis Broken
• Missed Abortion
• Hyperpituitarism
• Mosaic Trisomy 9
• Haddad Syndrome
• Hemimegalencephaly
• Anodontia of Permanent Teeth
• Selective Tooth Agenesis Type 5
• Selective Tooth Agenesis Type 3
• Selective Tooth Agenesis Type 4
• Selective Tooth Agenesis Type 1
• Anodontia
• Subcortical Band Heterotopia
• Nipah Virus Disease
• LIG4 Syndrome
• Autosomal Dominant Myoglobinuria
• Genetic Recurrent Myoglobinuria
• Hashimoto-Pritzker Syndrome
• Primary Parathyroid Hyperplasia
• Hyperparathyroidism-Jaw Tumor Syndrome
• Familial Isolated Hyperparathyroidism
• ACTH-Dependent Cushing Syndrome
• Gynandroblastoma
• Chronic Graft-Versus-Host-Disease
• Streptococcal Toxic-Shock Syndrome
• Placental-Site Trophoblastic Tumor
• Gestational Choriocarcinoma
• Malignant Placental Neoplasm
• Benign Recurrent Intrahepatic Cholestasis Type 1
• Dedifferentiated Liposarcoma
• Pleomorphic Liposarcoma
• Well-Differentiated Liposarcoma
• Klatskin Tumor
• Apnea of Prematurity
• Cerebral Amyloid Angiopathy
• Intraneural Perineurioma
• Amelogenesis Imperfecta Hypomaturation Type
• Primary Progressive Non-Fluent Aphasia
• Semantic Dementia
• Hereditary Angioedema Type 2
• Carcinoid Tumor and Carcinoid Syndrome
• Autosomal Recessive Spastic Paraplegia Type 25
• Peters Anomaly - Cataract Syndrome
• Familial Hypocalciuric Hypercalcemia Type 2
• Spinocerebellar Ataxia Type 22
• Metabolic Liver Disease
• Spotted Fever Rickettsiosis
• Typhus-Group Rickettsiosis
• Autosomal Recessive Limb-Girdle Muscular Dystrophy
• Pure Hereditary Spastic Paraplegia
• IgG Deficiency
• Intestinal Polyposis Syndrome
• Cerebrovascular Dementia
• Tauopathy
• Combined Deficiency of Vitamin K-Dependent Clotting Factors Type 2
• Combined Deficiency of Vitamin K-Dependent Clotting Factors Type 1
• Metabolic Myopathy
• Idiopathic Inflammatory Myopathy
• Idiopathic Interstitial Pneumonia
• Autosomal Dominant Nocturnal Frontal Lobe Epilepsy Type 3
• Congenital Anomaly of the Great Arteries
• Myopia Type 23
• Goniodysgenesis
• Vitreoretinal Degeneration
• Optic Atrophy Type 4
• Secondary Entropion
• Congenital Entropion
• Congenital Upper Palpebral Retraction
• Palpebral Nevus
• Syndromic Orbital Border Hypoplasia
• Conjunctival Lymphangiectasia
• Adult-Onset Foveomacular Vitelliform Dystrophy
• Reticular Dystrophy of the Retinal Pigment Epithelium
• Butterfly-Shaped Pigment Dystrophy
• Early-Onset Nuclear Cataract
• Primary Open-Angle Glaucoma Type 1N
• Juvenile-Onset Primary Open-Angle Glaucoma Type 3
• Juvenile-Onset Primary Open-Angle Glaucoma Type 2
• Chandler Syndrome
• Thiel-Behnke Corneal Dystrophy
• Coloboma of Eyelid
• Colobomatous Microphthalmia
• Miller-Fisher Syndrome
• Optic Atrophy Type 2
• Red Cell Aplasia
• Chronic Acquired Pure Red Cell Aplasia
• Autosomal Recessive Emery-Dreifuss Muscular Dystrophy
• Congenital Dyserythropoietic Anemia Type 3
• Southeast Asian Ovalocytosis
• Hereditary Pyropoikilocytosis
• Lymphomatoid Papulosis
• Lymphocyte-Rich Classical Hodgkin Lymphoma
• Aggressive Systemic Mastocytosis
• Atypical Chronic Myeloid Leukemia
• Acute Myeloid Leukemia with 11q23 Abnormalities
• Bilineal Acute Leukemia
• Primary Mediastinal Large B-Cell Lymphoma
• Familial Hypertrophic Cardiomyopathy
• Leber Hereditary Optic Neuropathy plus Disease
• Fried's Tooth and Nail Syndrome
• Metaphyseal Chondromatosis with D-2-Hydroxyglutaric Aciduria
• Dappled Diaphyseal Dysplasia
• Spondyloepimetaphyseal Dysplasia Type Handigodu
• Complete Androgen Insensitivity Syndrome
• Atlantoaxial Subluxation
• Fleck Retina of Kandori
• Acquired Von Willebrand Syndrome
• Multiple Ventricular Septal Defects
• Atrial Septal Defect Type Sinus venosus
• Atrial Septal Aneurysm
• Congenital Stenosis of the Inferior Vena Cava
• Aorto-Right Ventricular Tunnel
• Kommerell Diverticulum
• Persistent Fifth Aortic Arch
• Dysphagia Lusoria
• Cervical Aortic Arch
• Interventricular Septum Aneurysm
• Acquired Thrombotic Thrombocytopenic Purpura
• Autoinflammatory Syndrome
• Familial Thyroglossal Duct Cyst
• Neurofibromatosis Type 3
• Humero-Ulnar Synostosis
• Neovascular Glaucoma
• Uremic Pruritus
• Brachydactyly Type A4
• Brachydactyly Type C
• Brachydactyly Type B
• Brachydactyly Type B1
• Spondyloepimetaphyseal Dysplasia with Joint Laxity Type 1
• Bent Bone Dysplasia
• Acromesomelic Dysplasia
• Syndactyly Type 3
• Neonatal Osteosclerotic Dysplasia
• Dense Deposit Disease
• Levocardia
• Mosaic Trisomy 8
• Mosaic Trisomy 22
• 7q11.23 Duplication Syndrome
• Emanuel Syndrome
• Ring Chromosome 9
• Ring Chromosome 11 Syndrome
• Pseudohypoparathyroidism Type 1B
• Pseudohypoparathyroidism Type 2
• Hereditary Renal Hypouricemia
• Spinocerebellar Ataxia with Axonal Neuropathy
• Cerebellar Ataxia Type Cayman
• Angioma Serpiginosum
• Congenital Tracheomalacia
• Primary Progressive Aphasia
• Secondary Short Bowel Syndrome
• Congenital Disorder of Glycosylation Type 2H
• Congenital Malformation of the Tricuspid Valve
• Mesocardia
• Congenital Anomaly of Superior Vena Cava
• Anomalies of Great Veins, Congenital
• Atypical Arterial Duct
• Iatrogenic or Traumatic Pituitary Deficiency
• Acquired Premature Ovarian Failure
• Thyroid Dysgenesis
• Cytomegalic Congenital Adrenal Hypoplasia
• Congenital Non-Goitrous Hypothyroidism Type 3
• Congenital Renal Artery Stenosis
• Infectious Disease of the Nervous System
• Fingerprint Body Myopathy
• Chronic Conjunctivitis
• Solar Urticaria
• Zebra Body Myopathy
• Reducing Body Myopathy
• 48,XXXY Syndrome
• Ring Chromosome 13
• Ring Chromosome 15
• Idiopathic Membranous Glomerulonephritis
• Sinding-Larsen-Johansson Disease
• Furlong Syndrome
• Carney-Stratakis Syndrome
• Familial Papillary Thyroid Carcinoma with Papillary Renal Cell Carcinoma
• Congenital Muscular Dystrophy
• Acute Myeloid Leukemia with Recurrent Genetic Anomaly
• Mastocytosis
• Indolent Systemic Mastocytosis
• Postinfectious Encephalitis
• Infectious Encephalitis
• 46,XY Disorder of Sex Development
• Familial Digital Arthropathy - Brachydactyly
• Infantile Osteopetrosis with Neuroaxonal Dysplasia
• Autosomal Recessive Osteopetrosis Type 5
• Perineurioma
• Focal Segmental Glomerulosclerosis Type 4
• Neurogenic Scapuloperoneal Syndrome Type Kaeser
• Hypochromic Microcytic Anaemia with Iron Overload Type 1
• Fibronectin Glomerulopathy
• Hinman Syndrome
• Mycoplasma Encephalitis
• Congenital Primary Aphakia
• Microtia
• Florid Cemento-Osseous Dysplasia
• Immune Defect due to Absence of Thymus
• West Nile Virus Infection
• Desmoplastic Small Round Cell Tumor
• Pseudotyphus of California
• Punctate Palmoplantar Keratoderma Type 1
• Ichthyosis Hystrix Gravior
• Ichthyosis Hystrix Type Curth-Macklin
• Nasal-Type Extranodal NK-T-Cell Lymphoma
• Hepatosplenic T-cell Lymphoma
• Enteropathy-Associated T-Cell Lymphoma
• Nodular Lymphocyte-Predominant Hodgkin Lymphoma
• Alpha-Heavy Chain Disease
• Gamma-Heavy Chain Disease
• T-Cell Prolymphocytic Leukemia
• Aggressive NK-Cell Leukemia
• Adult T-Cell Leukemia - Lymphoma
• Acute Myeloid Leukemia with Multilineage Dysplasia
• Acute Basophilic Leukemia
• Acute Biphenotypic Leukemia
• B-Cell Prolymphocytic Leukemia
• Chronic Neutrophilic Leukemia
• Unclassified Chronic Myeloproliferative Disease
• Juvenile Myelomonocytic Leukemia
• Refractory Anemia with Excess Blasts
• Acute Panmyelosis with Myelofibrosis
• AMME Syndrome
• Congenital Analbuminemia
• Aplasia of Lacrimal and Salivary Glands
• Congenital Malformation of Salivary Glands and Ducts
• Agenesis of Lacrimal and Salivary Glands
• Hereditary Amyloidosis with Primary Renal Involement
• Familial Amyloid Polyneuropathy Type 4
• Juvenile Psoriatic Arthritis
• Systemic Juvenile Idiopathic Arthritis
• X-Linked Syndromic Mental Retardation Type Turner
• X-Linked Syndromic Mental Retardation Type 9
• X-Linked Syndromic Mental Retardation Type 12
• X-Linked Spinocerebellar Ataxia Type 4
• X-Linked Syndromic Mental Retardation Type Stocco dos Santos
• X-Linked Syndromic Mental Retardation Type Siderius
• X-Linked Syndromic Intellectual Disability Type Schimke
• Wieacker-Wolff Syndrome
• MEHMO Syndrome
• Microphthalmia - Ankyloblepharon - Intellectual Disability Syndrome
• X-Linked Syndromic Mental Retardation Type 7
• X-Linked Syndromic Intellectual Disability Type Abidi
• Genochondromatosis Type 1
• Spondylo-Ocular Syndrome
• Idiopathic Juvenile Osteoporosis
• Metaphyseal Dysplasia Type Braun-Tinschert
• Autosomal Dominant Chondrodysplasia Punctata
• Chondrodysplasia punctata Type Toriello
• Tibial-Metacarpal Chondrodysplasia Punctata
• 3-Phosphoglycerate Dehydrogenase Deficiency
• Erythrokeratoderma
• Congenital Disorder of Glycosylation Type 1F
• Congenital Disorder of Glycosylation Type 1G
• Congenital Disorder of Glycosylation Type 1H
• Congenital Disorder of Glycosylation Type 1L
• Congenital Disorder of Glycosylation Type 2E
• Niemann-Pick Disease Type D
• Akesson Syndrome
• Oculocutaneous Albinism Type 3
• Oculocutaneous Albinism Type 4
• Cutaneous Mastocytoma
• Diffuse Cutaneous Mastocytosis
• X-Linked Lethal Multiple Pterygium Syndrome
• Pretibial Dystrophic Epidermolysis Bullosa
• Woolly Hair Nevus
• Skin Vascular Disease
• Subcutaneous Tissue Disease
• Chronic Nephritic Syndrome with Dense Deposit Disease
• Cryoglobulinemic Vasculitis
• Gonadotropic Pituitary Adenoma
• Cardiomyopathy - Hypotonia - Lactic Acidosis Syndrome
• Isolated Congenital Sclerocornea
• Congenital Ectropion Uveae
• Pilomatrixoma
• Familial Capillary Hemangioma
• Isolated Congenital Alacrima
• Ring Dermoid of Cornea
• Familial Congenital Palsy of Trochlear Nerve
• Early-Onset Anterior Polar Cataract
• Coralliform Cataract
• Cerulean Cataract
• Persistent Hyperplastic Primary Vitreous
• Snowflake Vitreoretinal Degeneration
• Congenital Esophageal Diverticulum
• Secondary Ciliary Dyskinesia
• Congenital Horner Syndrome
• Marcus-Gunn Syndrome
• Acquired Angioedema
• ACE Inhibitor-Induced Angioedema
• Isolated Cryptophthalmia
• Mitochondrial Non-Syndromic Sensorineural Deafness
• Deafness - Hypogonadism Syndrome
• Orofaciodigital Syndrome Type 7
• Anonychia - Onychodystrophy Syndrome
• Telangiectasia Macularis Eruptiva Perstans
• Autosomal-Recessive Nonsyndromic Hearing Loss and Deafness DFNB61
• Deafness, Autosomal Dominant 23
• X-Linked Non-Syndromic Sensorineural Deafness Type DFN
• Disorder of Sex Development
• Brachyrachia
• Hypochondrogenesis
• Autosomal Recessive Spondyloepiphyseal Dysplasia Tarda
• Polysyndactyly
• Polydactyly of a Biphalangeal Thumb
• Postaxial Polydactyly Type A4
• Renal Dysplasia, Bilateral
• Pauci-Immune Glomerulonephritis
• Renal Cysts and Diabetes Syndrome
• Posterior Urethral Valve
• Unilateral Renal Hypoplasia
• Thanatophoric Dysplasia Type Glasgow
• Short Rib-Polydactyly Syndrome, Verma-Naumoff Type
• Crouzon Syndrome-Acanthosis Nigricans Syndrome
• Fragile X-Associated Tremor - Ataxia Syndrome
• Severe Infantile Polycystic Kidney Disease with Tuberous Sclerosis
• Langerhans Cell Sarcoma
• Follicular Dendritic Cell Sarcoma
• Dendritic Cell Sarcoma Not Otherwise Specified
• Idiopathic Hemiconvulsion-Hemiplegia Syndrome
• Myoclonic Epilepsy of Infancy
• Lymphedema - Cerebral Arteriovenous Anomaly Syndrome
• Sialidosis Type 2
• Autosomal Recessive Mental Retardation Type 34
• Autosomal Recessive Mental Retardation Type 28
• Autosomal Recessive Mental Retardation Type 25
• Autosomal Recessive Mental Retardation Type 24
• Autosomal Recessive Mental Retardation Type 23
• Autosomal Recessive Mental Retardation Type 19
• Autosomal Recessive Mental Retardation Type 30
• Autosomal Recessive Mental Retardation Type 33
• Autosomal Recessive Mental Retardation Type 29
• Autosomal Recessive Mental Retardation Type 18
• Autosomal Recessive Mental Retardation Type 16
• Autosomal Recessive Mental Retardation Type 14
• Autosomal Recessive Mental Retardation Type 4
• Autosomal Recessive Mental Retardation Type 11
• Autosomal Recessive Mental Retardation Type 10
• Autosomal Recessive Mental Retardation Type 9
• Autosomal Recessive Mental Retardation Type 7
• Autosomal Recessive Mental Retardation Type 6
• Autosomal Recessive Mental Retardation Type 12
• Autosomal Recessive Mental Retardation Type 1
• Familial Acute Necrotizing Encephalopathy
• Isolated Congenital Anosmia
• Tritanopia
• Ichthyosis-Prematurity Syndrome
• Superior Limbic Keratoconjunctivitis
• Familial Anterior Segment Mesenchymal Dysgenesis
• Hypomyelinating Leukodystrophy Type 8
• Amelogenesis Imperfecta
• Amelogenesis Imperfecta Type 1H
• Amelogenesis Imperfecta Type 2A4
• X-Linked Amelogenesis Imperfecta Type 2
• Amelogenesis Imperfecta Type 2A1
• Amelogenesis Imperfecta Type 3A
• Amelogenesis Imperfecta Type 4
• Charcot-Marie-Tooth Disease - Deafness - Intellectual Disability
• Invasive Infections due to Vancomycin-Resistant Enterococci
• Scarring in Glaucoma Filtration Surgical Procedures
• Autosomal Recessive Cutis Laxa Type 2
• Autosomal Recessive Cutis Laxa Type 1
• Xeroderma Pigmentosum Variant
• Early-Onset Sarcoidosis
• Warm Autoimmune Hemolytic Anemia
• IgG4-Related Hepatopathy
• Radiation Myelitis
• Guam Disease
• Deafness with Labyrinthine Aplasia - Microtia - Microdontia
• Moderate and Severe Traumatic Brain Injury
• Moderate and Severe Traumatic Cerebral Edema
• Hematopoietic Stem Cell Transplantation
• Acute Sensorineural Hearing Loss by Acute Acoustic Trauma
• Familial Pseudohyperkalemia
• Bacterial Sepsis of Newborn
• Sepsis of Newborn due to Other and Unspecified Streptococci
• Sepsis in Premature Infants
• Partial Deep Dermal and Full Thickness Burns
• Mitochondrial Disease
• Peroxisomal Disease
• Rare Inborn Errors of Metabolism
• Hereditary Persistence of Fetal Hemoglobin
• Bullous Systemic Lupus Erythematosus
• Cerebral Arteriovenous Malformation
• Papillary Renal Cell Carcinoma Type 1
• Idiopathic Neonatal Atrial Flutter
• Incessant Infant Ventricular Tachycardia
• Miyoshi Myopathy Type 2
• PHACE Syndrome
• Generalized Arterial Calcification of Infancy
• Kikuchi-Fujimoto Disease
• Keratolytic Winter Erythema
• Familial Short QT Syndrome
• Torsade-De-Pointes Syndrome with Short Coupling Interval
• Mesothelioma
• Malignant Mesothelioma
• Primary Effusion Lymphoma
• Lissencephaly
• Achromatopsia Type 4
• IgG4-Related Retroperitoneal Fibrosis
• Cornea Plana Type 2
• Cornea Plana Type 1
• Lethal Arthrogryposis - Anterior Horn Cell Disease Syndrome
• Cobb Syndrome
• Distal Spinal Muscular Atrophy
• Thrombotic Microangiopathy
• Posterior Cortical Atrophy
• Left Ventricular Noncompaction
• Hereditary Geniospasm
• Goldmann-Favre Syndrome
• Congenital Lactase Deficiency
• Isolated Follicle Stimulating Hormone Deficiency
• Systemic Vasculitis
• Familial Cutaneous Collagenoma
• MALT Lymphoma
• Inclusion Body Myopathy - Paget Disease - Frontotemporal Dementia Type 3
• Inclusion Body Myopathy - Paget Disease - Frontotemporal Dementia Type 2
• Corneal Dystrophies
• Familial Primary Hypomagnesemia with Normocalciuria and Normocalcemia
• Severe Idiopathic Pneumococcemia
• Idiopathic Disseminated Cytomegalovirus Infection
• Idiopathic Recurrent and Disabling Cutaneous Herpes
• Granulomatous Slack Skin
• Medullary Cystic Kidney Disease Type 2
• Combined Deficiency of Factors V - VIII Type 2
• Combined Deficiency of Factors V - VIII with Normal Protein C and Protein C Inhibitor
• Combined Deficiency of Factors V - VIII
• Familial Vascular Leukoencephalopathy
• Paraneoplastic Neurologic Syndrome
• Congenital Sucrase-Isomaltase Deficiency
• Epidermal Nevus Syndrome
• Isolated Synostotic Plagiocephaly
• Mitochondrial DNA Depletion Syndrome
• Madelung Deformity
• Coloboma of Optic Papilla
• Iminoglycinuria
• Bietti Crystalline Dystrophy
• Parasomnia
• Autoimmune Hypoparathyroidism
• Chronic Interstitial Cystitis
• Uveal Melanoma
• Acute graft versus host disease
• Müllerian Aplasia
• Retinal Dystrophy
• Psychogenic Movement Disorders
• Proopiomelanocortin Deficiency
• Cancer-Associated Retinopathy
• Familial Isolated Restrictive Cardiomyopathy
• Osteosclerosis-Ichthyosis-Premature Ovarian Failure Syndrome
• Central Neurocytoma
• Intestinal Lymphangiectasia
• Oguchi Disease Type 2
• Cystoid Macular Dystrophy
• Familial Drusen
• Progressive Bifocal Chorioretinal Atrophy
• North Carolina Macular Dystrophy
• Inclusion Body Myopathy Type 3
• Majeed Syndrome
• Syndromic Microphthalmia Type 10
• Respiratory Bronchiolitis Interstitial Lung Disease
• Acute Interstitial Pneumonia
• Hepatic Veno-Occlusive Disease-Immunodeficiency Syndrome
• Bickerstaff Brainstem Encephalitis
• Grange Syndrome
• Atrophodermia Vermiculata