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DO Term : Meckel syndrome 2 [DOID:0070116] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of the TMEM216 gene on chromosome 11q12.2.

synonyms:
603194,
Meckel-Gruber syndrome, type 2,
ICD10CM:Q61.9,
MKS2,
OMIM:603194

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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