Disease Index

Human disease

human disease

Atrophic lichen planus (LP) is a rare variant of cutaneous lichen planus (see this term) characterized by the development of pale papules or plaques with an atrophic center

Dermatological condition

Human disease

autism spectrum disorder that involves some autistic symptoms occuring after age 3 with an abscence of all the traits necessary for a diagnosis of autism

Human disease

myelodysplastic myeloproliferative neoplasm characterized by the principal involvement of the neutrophil series with leukocytosis and multilineage dysplasia

human disease

Gaucher's disease that has material basis in an autosomal recessive mutation of PSAP on chromosome 10q22.1

Atypical glycine encephalopathy is a rare form of glycine encephalopathy (GE; see this term) presenting disease onset or clinical manifestations that differ from neonatal or infantile GE

complement deficiency that is characterized by mechanical hemolytic anemia, thrombocytopenia, and renal dysfunction

human disease

human disease

human disease

human disease

human disease

human disease

human disease

human disease

human disease

medical condition

Human disease

human disease

human disease