Camptodactyly, myopia, and fibrosis of the medial rectus muscle of eye

Preferred Label : Camptodactyly, myopia, and fibrosis of the medial rectus muscle of eye;

Type : Other, mainly phenotypes with suspected mendelian basis;

Prefixed ID : 602612;

Details

Origin ID

602612;

UMLS CUI

C1865133;

Currated CISMeF NLP mapping
- camptodactyly, myopia, and fibrosis of the medial rectus muscle of eye [MeSH concept]
ORDO concept(s)
- Camptodactyly-joint contractures-facial skeletal defects syndrome [ORDO Disease]
See also inter- (CISMeF)
- Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder) [SNOMED CT concept]
- Camptodactyly-joint contractures-facial skeletal defects syndrome [ORDO Disease]
- Rozin Hertz Goodman syndrome [MeSH concept]
- rozin hertz goodman syndrome [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- camptodactyly, myopia, and fibrosis of the medial rectus muscle of eye [MeSH concept]

Keyword's position in hierarchy(ies) :

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