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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: Darier Disease (D007644)
..Starting node ..Darier Disease, Acral Hemorrhagic Type (C565125)
Child Nodes:
Sister Nodes:
..Burnett Schwartz Berberian syndrome (C537412)
..Darier Disease, Acral Hemorrhagic Type (C565125)
..Darier Disease, Segmental (C565126)
..Keratosis follicularis dwarfism cerebral atrophy (C536158)
..Keratosis Follicularis Spinulosa Decalvans, Autosomal Dominant (C567553)
..Kyrle disease (C538130)
..Van Den Bosch Syndrome (C563129)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	2972
Name:	Darier Disease, Acral Hemorrhagic Type
Definition:
Alternative IDs:
ParentIDs:	MESH:D007644
TreeNumbers:	C16.320.850.190/C565125 \|C17.800.428.275/C565125 \|C17.800.827.190/C565125
Synonyms:
Slim Mappings:	Genetic disease (inborn)\|Skin disease
Reference:	MedGen: C565125 MeSH: C565125 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants