WormMine

WS295

Intermine data mining platform for C. elegans and related nematodes

Ontology Relation :

Relationship  is_a Parent Term . Identifier  DOID:0080015
Child Term . Identifier  DOID:0070292 Direct  false
Redundant  false

1 Child Term

Identifier Name Description
DOID:0070292 primary autosomal recessive microcephaly 9 A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the CEP152 gene on chromosome 15q21.

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.