catel manzke syndrome

Preferred Label : catel manzke syndrome;

MeSH synonym : pierre robin syndrome with hyperphalangy and clinodactyly; hyperphalangy-clinodactyly of index finger with pierre robin syndrome; palatodigital syndrome, Catel-Manzke type; index finger anomaly with pierre robin syndrome; Catel-Manzke syndrome;

Details

Origin ID

C535347;

UMLS CUI

C1844887;

Automatic exact mappings (from CISMeF team)
- Catel Manzke syndrome [MedDRA Preferred Term]
- Catel-Manzke syndrome [ICD-11 More detail]
CISMeF manual mappings
- Catel Manzke syndrome (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Catel-Manzke syndrome [ORDO Disease]
- Catel-manzke syndrome [OMIM Phenotype]
- Catel-manzke syndrome [OMIM Phenotype]
Has phenotype(s) (HPO)
- High-arched palate [HPO term]
- Isolated cases [HPO term]
- Prenatal growth deficiency [HPO term]
MeSH term(s) associated for indexing
- hand deformities, congenital [MeSH Descriptor]
- pierre robin syndrome [MeSH Descriptor]
ORDO relation(s)
- Catel-Manzke syndrome [ORDO Disease]
Record concept(s)
- Catel Manzke syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Catel Manzke syndrome [MedDRA Preferred Term]
- Catel Manzke syndrome (disorder) [SNOMED CT concept]
- Catel-Manzke syndrome [ORDO Disease]
- Catel-manzke syndrome [OMIM Phenotype]
- Catel-manzke syndrome [OMIM Phenotype]

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