Tooth agenesis, selective, 8

Preferred Label : Tooth agenesis, selective, 8;

Symbol : STHAG8;

CISMeF acronym : STHAG8;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal dominant;

Molecular basis : Caused by mutation in the wingless-type MMTV integration site family, member-10B gene (WNT10B, 601906.0003);

Prefixed ID : #617073;

Details

Origin ID

617073;

UMLS CUI

C4310730;

Automatic exact mappings (from CISMeF team)
- WNT10B wt Allele [NCIt concept]
Genes related to phenotype
- Wingless-type mmtv integration site family, member 10b [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Dry skin [HPO term]
- Microdontia [HPO term]
- Selective tooth agenesis [HPO term]
- Sparse eyebrow [HPO term]
- Sparse hair [HPO term]
ORDO concept(s)
- Oligodontia [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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