Pyknoachondrogenesis

Preferred Label : Pyknoachondrogenesis;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal recessive;

Prefixed ID : 265880;

Details

Origin ID

265880;

UMLS CUI

C1849523;

Automatic exact mappings (from CISMeF team)
- Pyknoachondrogenesis [ICD-11 More detail]
Currated CISMeF NLP mapping
- Pyknoachondrogenesis [MeSH concept]
- Pyknoachondrogenesis [ORDO Disease]
- Pyknoachondrogenesis (disorder) [SNOMED CT concept]
- pyknoachondrogenesis [MeSH Supplementary Concept]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Increased bone mineral density [HPO term]
- Stillbirth [HPO term]
- Stillbirth [HPO term]
ORDO concept(s)
- Pyknoachondrogenesis [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Pyknoachondrogenesis [ORDO Disease]
- Pyknoachondrogenesis [MeSH concept]
- Pyknoachondrogenesis (disorder) [SNOMED CT concept]
- pyknoachondrogenesis [MeSH Supplementary Concept]

Keyword's position in hierarchy(ies) :

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