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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