Disease Index
9,486 diseasesgeleophysic dysplasia
disease
MeSH: C537677
Gemignani syndrome
human disease
MeSH: C537678
gemistocytic astrocytoma
human disease
Generalized atrophic benign epidermolysis bullosa
generalized basaloid follicular hamartoma syndrome
human disease
generalized bulbospinal muscular atrophy
human disease
Generalized dominant dystrophic epidermolysis bullosa
generalized epidermolysis bullosa simplex
epidermolysis bullosa simplex that is characterized by widespread blisters that appear at birth or in early infancy
MeSH: C535961
generalized epilepsy with febrile seizures plus
idiopathic generalized epilepsy that is characterized by febrile seizures often with accessory afebrile generalized tonic-clonic seizures with childhood onset
MeSH: C565809
generalized epilepsy-paroxysmal dyskinesia syndrome
gene (chromosome 10q22), encoding the alpha subunit of the BK channel. Transmission is autosomal dominant.
MeSH: C563719
generalized eruptive histiocytoma
human disease
generalized eruptive keratoacanthoma
Generalized essential telangiectasia
medical condition
generalized galactose epimerase deficiency
human disease
generalized isolated dystonia
human disease
Generalized lentiginosis
Medical condition.
ICD: L81.4MeSH: C573023
generalized peeling skin syndrome type c
human disease
generalized pustular psoriasis
human disease
ICD: L40.1
generalized resistance to thyroid hormone
human disease
genetic alopecia
instance of alopecia that is caused by a modification of the individual's genome
genetic biliary tract disease
Genetic biliary tract disease
genetic cardiac anomaly
human disease
genetic cardiac disease
rare genetic heart disease
genetic cardiac malformation
human disease
genetic cardiac rhythm disease
instance of cardiac rhythm disease that is caused by a modification of the individual's genome
genetic cardiac tumor
Genetic heart cancer
genetic central nervous system and retinal vascular disease
human disease
genetic cerebral small vessel disease
human disease
genetic dementia
Genetic dementia
genetic endocrine growth disease
human disease