WormMine

WS296

Intermine data mining platform for C. elegans and related nematodes

Ontology Relation :

Relationship  is_a Parent Term . Identifier  DOID:16
Child Term . Identifier  DOID:0070134 Direct  false
Redundant  false
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1 Child Term

Identifier Name Description
DOID:0070134 autosomal recessive cutis laxa type IIA An autosomal recessive cutis laxa type II classic type that has_material_basis_in homozygous or compound heterozygous mutations in the ATP6V0A2 gene on chromosome 12q24.

1 Parent Term

Identifier Name Description
DOID:16 integumentary system disease A disease of anatomical entity that is located_in the integumentary system comprising the skin and its appendages.