WormMine

WS296

Intermine data mining platform for C. elegans and related nematodes

Ontology Relation :

Relationship  is_a Parent Term . Identifier  DOID:0080015
Child Term . Identifier  DOID:0110881 Direct  false
Redundant  false

1 Child Term

Identifier Name Description
DOID:0110881 holoprosencephaly 1 A holoprosencephaly that has_material_basis_in variation in the chromosome region 21q22.3.

1 Parent Term

Identifier Name Description
DOID:0080015 physical disorder A disease that has_material_basis_in a genetic abnormality, error with embryonic development, infection or compromised intrauterine environment.