WormMine

WS295

Intermine data mining platform for C. elegans and related nematodes

Ontology Relation :

Relationship  is_a Parent Term . Identifier  DOID:4
Child Term . Identifier  DOID:0070116 Direct  false
Redundant  false
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1 Child Term

Identifier Name Description
DOID:0070116 Meckel syndrome 2 A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of the TMEM216 gene on chromosome 11q12.2.

1 Parent Term

Identifier Name Description
DOID:4 disease A disease is a disposition (i) to undergo pathological processes that (ii) exists in an organism because of one or more disorders in that organism.