Parietal foramina 3

Preferred Label : Parietal foramina 3;

Symbol : PFM3;

CISMeF acronym : PFM3;

Type : Phenotype or locus, molecular basis unknown;

Description : For a phenotypic description and a discussion of genetic heterogeneity of parietal foramina (PFM), see 168500.;

Inheritance : Autosomal dominant;

Prefixed ID : %609566;

Details

Origin ID

609566;

UMLS CUI

C1835980;

Broader ORDO disease(s)
- Enlarged parietal foramina [ORDO Disease]
Currated CISMeF NLP mapping
- parietal foramina 3 [MeSH concept]
- parietal foramina 3 [MeSH Supplementary Concept]
DO Cross reference
- parietal foramina [DO Concept]
HPO term(s)
- Aplasia cutis congenita of scalp [HPO term]
- Autosomal dominant inheritance [HPO term]
- Encephalocele [HPO term]
- Heterogeneous [HPO term]
- Parietal foramina [HPO term]
- Symmetrical, oval parietal bone defects [HPO term]
ORDO concept(s)
- Enlarged parietal foramina [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- parietal foramina 3 [MeSH Supplementary Concept]
- parietal foramina 3 [MeSH concept]
Validated automatic mappings to NTBT
- parietal foramina [DO Concept]

Keyword's position in hierarchy(ies) :

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