WormMine

WS295

Intermine data mining platform for C. elegans and related nematodes

Ontology Relation :

Relationship  is_a Parent Term . Identifier  DOID:5679
Child Term . Identifier  DOID:0110189 Direct  false
Redundant  false
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1 Child Term

Identifier Name Description
DOID:0110189 Leber congenital amaurosis 15 A Leber congenital amaurosis that has_material_basis_in mutation in the TULP1 gene on chromosome 6p21.3.

1 Parent Term

Identifier Name Description
DOID:5679 retinal disease An eye disease that is located_in the retina.