robinow syndrome, autosomal recessive

Preferred Label : robinow syndrome, autosomal recessive;

Origin ID

C535863;

UMLS CUI

C1849334;

Currated CISMeF NLP mapping
- Autosomal recessive Robinow syndrome [ICD-11 More detail]
- Autosomal recessive Robinow syndrome [ORDO Disease]
- Autosomal recessive Robinow syndrome (disorder) [SNOMED CT concept]
- Robinow syndrome, autosomal recessive 1 [OMIM Phenotype]
- autosomal recessive Robinow syndrome [DO Concept]
MeSH term(s) associated for indexing
- limb deformities, congenital [MeSH Descriptor]
- maxillofacial abnormalities [MeSH Descriptor]
- spine [MeSH Descriptor]
ORDO relation(s)
- Autosomal recessive Robinow syndrome [ORDO Disease]
Record concept(s)
- Robinow syndrome, autosomal recessive [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal recessive Robinow syndrome [ORDO Disease]
- Autosomal recessive Robinow syndrome (disorder) [SNOMED CT concept]
- Robinow syndrome, autosomal recessive 1 [OMIM Phenotype]
- autosomal recessive Robinow syndrome [DO Concept]