cutis laxa with severe pulmonary, gastrointestinal, and urinary abnormalities

Preferred Label : cutis laxa with severe pulmonary, gastrointestinal, and urinary abnormalities;

UMLS semantic type : T047 - Disease or Syndrome;

Details

Origin ID

M0568016;

UMLS CUI

C2750804;

Currated CISMeF NLP mapping
- Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies [ORDO Disease]
- Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies [ICD-11 More detail]
- Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies (disorder) [SNOMED CT concept]
- Cutis laxa, autosomal recessive, type ic [OMIM Phenotype]
- autosomal recessive cutis laxa type IC [DO Concept]
Related record
- cutis laxa with severe pulmonary, gastrointestinal, and urinary abnormalities [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies [ORDO Disease]
- Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies [ICD-11 More detail]
- Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies (disorder) [SNOMED CT concept]
- Cutis laxa, autosomal recessive, type ic [OMIM Phenotype]
- autosomal recessive cutis laxa type IC [DO Concept]

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