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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
autosomal recessive cutis laxa type IA  
autosomal recessive cutis laxa type IB  
An autosomal recessive cutis laxa type I characterized by disturbed elastic fiber formation resulting in severe systemic connective tissue abnormalities that has_material_basis_in homozygous or compound heterozygous mutation in the EFEMP2 gene on chromosome 11q13. (DO)
autosomal recessive cutis laxa type IC  
CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE 1D  

Synonyms
Exact Synonyms: ARCL1B ;   AUTOSOMAL RECESSIVE CUTIS LAXA TYPE 1B
Primary IDs: MIM:614437
Alternate IDs: RDO:9000260
Definition Sources: PMID:16685658 "DO" "DO", PMID:19664000 "DO" "DO"

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