OBO ID: DOID:0070136
Term Name: autosomal dominant cutis laxa 2 Search Ontology:
Synonyms:
  • ADCL2
Definition: An autosomal dominant cutis laxa that has_material_basis_in heterozygous mutation in the FBLN5 gene on chromosome 14q32. https://www.ncbi.nlm.nih.gov/pubmed/12618961
References:
Ontology: Human Disease   ( DOID:0070136 )
Relationships
is a type of:
OTHER autosomal dominant cutis laxa 2 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
FBLN5 ?Cutis laxa, autosomal dominant 2 614434
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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