WormMine

WS295

Intermine data mining platform for C. elegans and related nematodes

Ontology Relation :

Relationship  is_a Parent Term . Identifier  DOID:854
Child Term . Identifier  DOID:0080987 Direct  false
Redundant  false
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1 Child Term

Identifier Name Description
DOID:0080987 Ehlers-Danlos syndrome periodontal type 2 An Ehlers-Danlos syndrome that has_material_basis_in heterozygous mutation in the C1S gene on chromosome 12p13.

1 Parent Term

Identifier Name Description
DOID:854 collagen disease A connective tissue disease that characterized by connective tissue disease that has_material_basis_in inheritable defects in collagen.