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DO Term : autosomal dominant cutis laxa 1 [DOID:0070130] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An autosomal dominant cutis laxa that has_material_basis_in heterozygous mutations in the ELN gene on chromosome 7q11.

synonyms:
ICD10CM:Q82.8,
123700,
OMIM:123700,
ADCL1

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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