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16901 to 17000 most common queries
List represents a sample of symptoms, diseases, and other queries. Updated weekly.
Retroverted Uterus
Progressive Familial Intrahepatic Cholestasis 4
Chronic Cervicitis
Bulbourethral Gland Abscess
Hawkinsinuria
Lower Urinary Tract Infection
Split Hand-Split Foot Malformation Type 1
Acute Nephritis
Congenital Disorder of Glycosylation Type 2A
Congenital Disorder of Glycosylation Type 1K
Congenital Disorder of Glycosylation Type 1J
Congenital Disorder of Glycosylation Type 1C
Benign Essential Blepharospasm
Adrenal Gland Disease
Autosomal Recessive Deafness 88
Adrenal Hemorrhage
Adrenal Destruction
Autosomal Recessive Spastic Paraplegia Type 46
Hypertrophy of the Adrenal Cortex
Xeroderma Pigmentosum Complementation Group C
Osteopenia and Osteoporosis
Hereditary Sensory and Autonomic Neuropathy Type 2A
Purpura
Adrenal Cortex Disease
Giacheti Syndrome
Folate-Deficiency Anemia
Glycogen Storage Disease due to Muscle Beta-Enolase Deficiency
Congenital Disorder of Glycosylation Type 1T
Autosomal Recessive Spastic Paraplegia Type 50
Adolescence
Autosomal Recessive Cutis Laxa Type 2B
Retinitis Pigmentosa 42
Tics
Spastic Quadriplegic Cerebral Palsy Type 1
Adjustment Reaction of Adolescence
Myoadenylate Deaminase Deficiency
Intestinal Adhesions
Overeating
Pudendal Hernia
Epileptic Encephalopathy with Global Cerebral Demyelination
Chronic Appendicitis
Congenital Deafness
Ileal Crohn Disease
Cataract
Autosomal Recessive Parkinson Disease 14
Congenital Spinal Cord Anomaly
Froehlich's Syndrome
Myofibrillar Myopathy Type 6
Uterine Hypoplasia
Obesity
Optic Atrophy Type 7
Autosomal Dominant Emery-Dreifuss Muscular Dystrophy
Esophageal Duplication
Cleft Uvula
Mesenteric Lymphadenitis
Generalized Epilepsy with Febrile Seizures Plus Type 7
Viral Gastroenteritis
Santos Syndrome
Chromosome 19q13.11 Deletion Syndrome
Glycogen Storage Disease due to Liver Phosphorylase Kinase Deficiency
Upper Respiratory Infection
Genetic Combined Pituitary Hormone Deficiencies
Neurodegenerative Syndrome due to Cerebral Folate Transport Deficiency
Iritis
Platelet-Type Bleeding Disorder 12
Viral Pneumonia
TTR Amyloidosis with Polyneuropathy
Bronchiolitis
Bronchiectasis with or without Elevated Sweat Chloride 3
Epidemic Keratoconjunctivitis
Hemivertebra
Acute Laryngitis
Autosomal Dominant Progressive External Ophthalmoplegia Type 5
Congenital Metatarsus Varus
Leukopenia
Basilar Artery Thrombosis
Basilar Artery Occlusion
Familial Juvenile Hyperuricemic Nephropathy Type 2
Internal Hemorrhoids
Cone Dystrophy Type 4
Ruptured Sinus of Valsalva
Acute Infectious Lymphocytosis
Hallux Rigidus
Acute Myocarditis
Hereditary Hypotrichosis with Recurrent Skin Vesicles
Achilles Tendon Rupture
Ischemic Ulcer
TUBB1-Related Autosomal Dominant Macrothrombocytopenia
Vagina Carcinoma
Hereditary Sensory and Autonomic Neuropathy Type 2B
Carcinoma of Ampulla of Vater
Adenovirus Infection
Prostatism
Severe Combined Immunodeficiency
Infantile Dystonia - Parkinsonism
Adenosine Deaminase Deficiency
Inflammatory Bowel Disease Type 28
Muscular Dystrophy-Dystroglycanopathy Type B4
Herniated Disc
Angina Pectoris