Disease Index

Rare genetic syndromic intellectual disability

human disease

instance of systemic or rheumatic disease that is caused by a modification of the individual's genome

human disease

instance of vascular anomaly that is caused by a modification of the individual's genome

rare genetic vascular disease

human disease

Genetic infertility

Genetic obesity

disorder that is caused by the reactivation of varicella zoster virus in the geniculate ganglion, a nerve cell bundle of the facial nerve

Hereditary geniospasm is a movement disorder characterized by episodes of involuntary tremor of the chin and lower lip

human disease

medical condition

skin disease that is caused by a modification of the individual's genome

human disease

deformity in the knee joint

human disease

medical condition

disease

germ cell cancer that lacks histologic differentiation, usually a brain tumor

human disease

nervous system disease that results from damage located in left parietal lobe, has symptom agraphia, has symptom acalculia, has symptom finger agnosia

prion disease characterized by adult onset of memory loss, dementia, ataxia, and pathologic deposition of amyloid-like plaques in the brain

Human disease

disease

Human disease