Disease Index
9,486 diseasesfilamin-related bone disorder
human disease
filarial elephantiasis
human disease caused by parasitic worms
MeSH: D004605
filariasis
parasitic disease caused by a family of nematode worms
MeSH: D005368
Filippi syndrome
MeSH: C538152
Fine-Lubinsky syndrome
Fine-Lubinsky syndrome is characterised by psychomotor delay, brachycephaly with flat face, small nose, microstomia, cleft palate, cataract, hearing loss, hypoplastic scrotum and digital anomalies
MeSH: C537933
finger hyperphalangy-toe anomalies-severe pectus excavatum syndrome
human disease
fingerprint body myopathy
disease
MeSH: C564425
Finnish upper limb-onset distal myopathy
rare genetic disease
first branchial cleft anomaly
human disease
Fish-eye disease
MeSH: C538467
Fitzsimmons–Guilbert syndrome
medical condition
MeSH: C537938
fixed drug reaction
human disease
ICD: L27.1
fixed subaortic stenosis
flat face-microstomia-ear anomaly syndrome
human disease
MeSH: C537339
Flea-borne spotted fever
medical condition
ICD: A77.8
fleck corneal dystrophy
human disease
MeSH: C563256
Floating-Harbor syndrome
genetic developmental disorder characterized by facial dysmorphism, short stature with delayed bone age, and expressive language delay
ICD: Q87.8MeSH: C537062
florid cemento-osseous dysplasia
MeSH: C537063
FLOTCH syndrome
human disease
MeSH: C537065
Flynn–Aird syndrome
medical condition
MeSH: C537066
focal acral hyperkeratosis
human disease
focal cortical dysplasia
human disease
ICD: Q04.6MeSH: D000092222
focal dermal hypoplasia
form of ectodermal dysplasia
ICD: Q82.8MeSH: D005489
focal dystonia
dystonia that is localized to a specific part of the body
focal epilepsy-intellectual disability-cerebro-cerebellar malformation
focal facial dermal dysplasia
heterogenous group of genetic disorders characterized by scar-like atrophic lesions on the temple
MeSH: D000090303
focal facial dermal dysplasia type II
Focal facial dermal dysplasia type II (FFDD2) is a focal facial dermal dysplasia (FFDD; see this term), characterized by congenital bitemporal scar-like depressions and other facial and organ abnormalities
focal facial dermal dysplasia type IV
Focal facial dermal dysplasia type IV (FFDD4) is a rare focal facial dysplasia (FFDD; see this term), characterized by congenital isolated preauricular and/or cheek blister scar-like lesions
focal myositis
Focal myositis is a rare inflammatory myopathy characterized by a localized swelling of skeletal muscle that is usually located in the lower extremities
focal or diffuse nonepidermolytic palmoplantar keratoderma
human disease