Search Ontology:
Human Disease
autosomal dominant cutis laxa 1
- Term ID
- DOID:0070130
- Synonyms
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- ADCL1
- Definition
- An autosomal dominant cutis laxa that has_material_basis_in heterozygous mutations in the ELN gene on chromosome 7q11. (2)
- References
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- ICD10CM:Q82.8
- OMIM:123700
- Ontology
- Human Disease ( DOID:0070130 )
- is a type of
-
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