Patella aplasia-hypoplasia

Preferred Label : Patella aplasia-hypoplasia;

Symbol : PTLAH;

CISMeF acronym : PTLAH;

Type : Phenotype or locus, molecular basis unknown;

Inheritance : Autosomal dominant;

Prefixed ID : %168860;

Details

Origin ID

168860;

UMLS CUI

C1868577;

Currated CISMeF NLP mapping
- Patella aplasia/hypoplasia [ORDO Disease]
HPO term(s)
- Abnormality of the skin [HPO term]
- Autosomal dominant inheritance [HPO term]
- Patellar aplasia [HPO term]
- Patellar hypoplasia [HPO term]
ORDO concept(s)
- Patella aplasia/hypoplasia [ORDO Disease]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Absent patella [MeSH concept]
- Aplasia/Hypoplasia of the patella [HPO term]
- Patella aplasia/hypoplasia [ORDO Disease]
- absent patella [MeSH Supplementary Concept]

Keyword's position in hierarchy(ies) :

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