WormMine

WS295

Intermine data mining platform for C. elegans and related nematodes

Ontology Relation :

Relationship  is_a Parent Term . Identifier  DOID:74
Child Term . Identifier  DOID:0111052 Direct  false
Redundant  false

1 Child Term

Identifier Name Description
DOID:0111052 Scott syndrome A blood coagulation disease characterized by autosomal recessive inheritance of hemorrhagic episodes due to impaired platelet coagulant activity that has_material_basis_in homozygous mutation in the TMEM16F gene on chromosome 12q12.

1 Parent Term

Identifier Name Description
DOID:74 hematopoietic system disease A disease of anatomical entity that has_material_basis_in hematopoietic cells.