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DO Term : Meckel syndrome 1 [DOID:0070115] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of the MKS1 gene on chromosome 17q22.

synonyms:
MKS1,
ICD10CM:Q61.9,
Meckel-Gruber syndrome, type 1,
249000,
OMIM:249000

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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