tel hashomer camptodactyly syndrome

Preferred Label : tel hashomer camptodactyly syndrome;

MeSH note : Camptodactyly with muscular hypoplasia, skeletal dysplasia, and abnormal palmar creases;

Details

Origin ID

C536953;

UMLS CUI

C1859356;

CISMeF manual mappings
- Tel Hashomer camptodactyly syndrome (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Camptodactyly with muscular hypoplasia, skeletal dysplasia, and abnormal palmar creases [OMIM Phenotype]
- Tel Hashomer camptodactyly syndrome [ORDO Disease]
MeSH term(s) associated for indexing
- dermatoglyphics [MeSH Descriptor]
- hand deformities, congenital [MeSH Descriptor]
- heart septal defects, atrial [MeSH Descriptor]
- hirsutism [MeSH Descriptor]
- muscular diseases [MeSH Descriptor]
ORDO relation(s)
- Tel Hashomer camptodactyly syndrome [ORDO Disease]
Record concept(s)
- Tel Hashomer camptodactyly syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Camptodactyly with muscular hypoplasia, skeletal dysplasia, and abnormal palmar creases [OMIM Phenotype]
- Tel Hashomer camptodactyly syndrome [ORDO Disease]
- Tel Hashomer camptodactyly syndrome (disorder) [SNOMED CT concept]

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