WormMine

WS297

Intermine data mining platform for C. elegans and related nematodes

Ontology Relation :

Relationship  is_a Parent Term . Identifier  DOID:630
Child Term . Identifier  DOID:0070006 Direct  false
Redundant  false

1 Child Term

Identifier Name Description
DOID:0070006 Seckel syndrome 6 A Seckel syndrome that has_material_basis_in homozygous mutation in the CEP63 gene on chromosome 3q22.

1 Parent Term

Identifier Name Description
DOID:630 genetic disease A disease that has_material_basis_in genetic variations in the human genome.