cutis laxa, autosomal recessive, type IIB

Preferred Label : cutis laxa, autosomal recessive, type IIB;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0568155;

UMLS CUI

C2751987;

Currated CISMeF NLP mapping
- Autosomal recessive cutis laxa type 2B [ORDO Disease]
- Autosomal recessive cutis laxa type 2B (disorder) [SNOMED CT concept]
- Autosomal recessive cutis laxa, type 2B [ICD-11 More detail]
- Cutis laxa, autosomal recessive, type iib [OMIM Phenotype]
- autosomal recessive cutis laxa type IIB [DO Concept]
- autosomal recessive cutis laxa type IIB [Disease (Nov.)]
Related record
- cutis laxa, autosomal recessive, type IIB [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal recessive cutis laxa type 2B [ORDO Disease]
- Autosomal recessive cutis laxa type 2B (disorder) [SNOMED CT concept]
- Autosomal recessive cutis laxa, type 2B [ICD-11 More detail]
- Cutis laxa, autosomal recessive, type iib [OMIM Phenotype]
- autosomal recessive cutis laxa type IIB [DO Concept]
- autosomal recessive cutis laxa type IIB [Disease (Nov.)]