Polydactyly, postaxial, with progressive myopia

Preferred Label : Polydactyly, postaxial, with progressive myopia;

CISMeF acronym : PMS;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : PMS; Polydactyly-myopia syndrome;

Inheritance : Autosomal dominant;

Prefixed ID : 174310;

Details

Origin ID

174310;

UMLS CUI

C1868117;

Automatic exact mappings (from CISMeF team)
- PREMENSTRUAL SYNDROME [WHO-ART Included Term]
- Picometer [NCIt concept]
- Picomole/liter (qualifier value) [SNOMED CT concept]
- Premenstrual tension syndrome (disorder) [SNOMED CT concept]
- premenstrual syndrome [MedlinePlus Topic]
Currated CISMeF NLP mapping
- Polydactyly myopia syndrome [MeSH concept]
- Polydactyly myopia syndrome (disorder) [SNOMED CT concept]
- Polydactyly-myopia syndrome [ORDO Disease]
- polydactyly myopia syndrome [MeSH Supplementary Concept]
False automatic mappings
- Saint Pierre and Miquelon [NCIt concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Myopia [HPO term]
- Postaxial hand polydactyly [HPO term]
- Progressive myopia [HPO term]
ORDO concept(s)
- Polydactyly-myopia syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Polydactyly myopia syndrome [MeSH concept]
- Polydactyly myopia syndrome (disorder) [SNOMED CT concept]
- Polydactyly-myopia syndrome [ORDO Disease]
- polydactyly myopia syndrome [MeSH Supplementary Concept]

Keyword's position in hierarchy(ies) :

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