Search Ontology:
Human Disease
autosomal recessive cutis laxa type IC
- Term ID
- DOID:0070139
- Synonyms
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- 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
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- MESH:C567716
- MIM:613177
- ORDO:221145
- SNOMEDCT_US_2023_03_01:784349004
- UMLS_CUI:C2750804
- Ontology
- Human Disease ( DOID:0070139 )
- is a type of
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Genes Involved
Zebrafish Models