WormMine

WS295

Intermine data mining platform for C. elegans and related nematodes

Ontology Relation :

Relationship  is_a Parent Term . Identifier  DOID:2121
Child Term . Identifier  DOID:0111342 Direct  true
Redundant  false

1 Child Term

Identifier Name Description
DOID:0111342 dermatopathia pigmentosa reticularis An ectodermal dysplasia characterized by reticulate hyperpigmentation, noncicatricial alopecia, and onychodystrophy that has_material_basis_in heterozygous mutation in the KRT14 gene on chromosome 17q21.2.

1 Parent Term

Identifier Name Description
DOID:2121 ectodermal dysplasia A syndrome characterized by abnormal development in 2 or more ectodermal structures (hair, nails, teeth, and sweat glands) without other systemic findings.