WormMine

WS295

Intermine data mining platform for C. elegans and related nematodes

Ontology Relation :

Relationship  is_a Parent Term . Identifier  DOID:17
Child Term . Identifier  DOID:0110210 Direct  false
Redundant  false

1 Child Term

Identifier Name Description
DOID:0110210 Charcot-Marie-Tooth disease X-linked recessive 5 A Charcot-Marie-Tooth disease X-linked that has_material_basis_in loss-of-function mutation in the PRPS1 gene on chromosome Xq22.

1 Parent Term

Identifier Name Description
DOID:17 musculoskeletal system disease A disease of anatomical entity that occurs in the muscular and/or skeletal system.