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DO Term : autosomal recessive cutis laxa type IIIA [DOID:0070132] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A autosomal recessive cutis laxa type III that has_material_basis_in homozygous mutation in the ALDH18A1 gene on chromosome 10q24.

synonyms:
ICD10CM:Q82.8,
ORDO:35664,
De Barsy syndrome A,
OMIM:219150,
219150,
ARCL3A

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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