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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
Annular Epidermolytic Ichthyosis +   
epidermolytic hyperkeratosis 1  
epidermolytic hyperkeratosis 2  
An epidermolytic hyperkeratosis that is characterized by generalized erythema, erosions, scaling, and easily breaking blisters that become less frequent later in life, while hyperkeratosis increases and that has_material_basis_in heterozygous or homozygous mutation in the keratin-10 gene (KRT10) on chromosome 17q21. (DO)
Epidermolytic Hyperkeratosis, Late-Onset 

Synonyms
Exact Synonyms: EHK2
Narrow Synonyms: EHK2A ;   EHK2B ;   epidermolytic hyperkeratosis 2A, autosomal dominant ;   epidermolytic hyperkeratosis 2B, autosomal recessive
Alternate IDs: DOID:9004068
Xrefs: MIM:620150 ;   MIM:620707 ;   MONDO:0958184
Definition Sources: PMID:19474805 "DO" "DO"

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