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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, Segmental (C565126)
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:	2973
Name:	Darier Disease, Segmental
Definition:
Alternative IDs:
ParentIDs:	MESH:D007644
TreeNumbers:	C16.320.850.190/C565126 \|C17.800.428.275/C565126 \|C17.800.827.190/C565126
Synonyms:
Slim Mappings:	Genetic disease (inborn)\|Skin disease
Reference:	MedGen: C565126 MeSH: C565126 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants