WormMine

WS295

Intermine data mining platform for C. elegans and related nematodes

Ontology Relation :

Relationship  is_a Parent Term . Identifier  DOID:225
Child Term . Identifier  DOID:0070365 Direct  false
Redundant  false

1 Child Term

Identifier Name Description
DOID:0070365 nevoid basal cell carcinoma syndrome 1 A nevoid basal cell carcinoma syndrome that has_material_basis_in heterozygous mutation in the PTCH1 gene on chromosome 9q22.

1 Parent Term

Identifier Name Description
DOID:225 syndrome A disease characterized by a group of signs and symptoms that occur together and characterize a particular abnormality.