Disease browser and phenotype portal

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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Disease Browser
Parent Node: Hair Diseases (D006201)
Parent Node: Virilism (D014770)
..Starting node ..Hirsutism (D006628)
Child Nodes:
........Acanthosis nigricans muscle cramps acral enlargement (C536000)
........Barber Say syndrome (C537908)
........Cortisone reductase deficiency (C536447)
........Spondyloepimetaphyseal dysplasia, Genevieve type (C535785)
........Tel Hashomer camptodactyly syndrome (C536953)
........Wiedemann Oldigs Oppermann syndrome (C536705)
Sister Nodes:
..Achard-Thiers syndrome (C536013)
..Hirsutism (D006628) 6
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	5205
Name:	Hirsutism
Definition:	A condition observed in WOMEN and CHILDREN when there is excess coarse body hair of an adult male distribution pattern, such as facial and chest areas. It is the result of elevated ANDROGENS from the OVARIES, the ADRENAL GLANDS, or exogenous sources. The concept does not include HYPERTRICHOSIS, which is an androgen-independent excessive hair growth.
Alternative IDs:
ParentIDs:	MESH:D006201\|MESH:D014770
TreeNumbers:	C17.800.329.750 \|C23.888.971.468
Synonyms:
Slim Mappings:	Signs and symptoms\|Skin disease
Reference:	MedGen: D006628 MeSH: D006628 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants