Search Ontology:
Human Disease

autosomal dominant cutis laxa 2

Term ID
DOID:0070136
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 Pages
Alliance (1)
Genes Involved
Zebrafish Models
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