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DO Term : arthrogryposis multiplex congenita-4 [DOID:0080980] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An arthrogryposis multiplex congenita that has_material_basis_in homozygous mutation in the SCYL2 gene on chromosome 12q23.

synonyms:
618766,
OMIM:618766,
Zain syndrome

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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