Search Ontology:
Human Disease

autosomal recessive cutis laxa type IC

Term ID
DOID:0070139
Synonyms
  • ARCL1C
  • autosomal recessive cutis laxa type 1C
Definition
A autosomal recessive cutis laxa type I that has_material_basis_in homozygous or compound heterozygous mutation in the LTBP4 gene on chromosome 19q13. https://www.ncbi.nlm.nih.gov/pubmed/19836010
References
Ontology
Human Disease   ( DOID:0070139 )
Relationships
is a type of
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Genes Involved
Zebrafish Models