Tooth agenesis, selective, 4

Preferred Label : Tooth agenesis, selective, 4;

Symbol : STHAG4;

CISMeF acronym : STHAG4;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Lateral incisors, absence of; Tooth agenesis, selective, 4, with or without ectodermal dysplasia; Lateral incisors, pegged or missing; Succedaneous teeth, agenesis of;

Inheritance : Autosomal dominant; Autosomal recessive;

Molecular basis : Caused by mutation in the wingless-type MMTV integration site family, member 10A gene (WNT10A, 606268.0002);

Prefixed ID : #150400;

Détails

Origin ID

150400;

UMLS CUI

C1835492;

Automatic exact mappings (from CISMeF team)
- Agenesis of lateral incisor [HPO term]
- Hypodontia [ORDO Disease]
- Oligodontia [ORDO Disease]
- WNT10A wt Allele [NCIt concept]
- succedaneous teeth, agenesis of [MeSH concept]
Broader ORDO disease(s)
- Hypodontia [ORDO Disease]
Currated CISMeF NLP mapping
- tooth agenesis, selective, 4 [MeSH concept]
- tooth agenesis, selective, 4 [MeSH Supplementary Concept]
DO Cross reference
- tooth agenesis [DO Concept]
Genes related to phenotype
- Wingless-type mmtv integration site family, member 10a [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Autosomal recessive inheritance [HPO term]
- Dry skin [HPO term]
- Peg-shaped maxillary lateral incisors [HPO term]
- Short eyelashes [HPO term]
- Sparse eyebrow [HPO term]
- Sparse hair [HPO term]
- Tooth agenesis [HPO term]
ORDO concept(s)
- Hypodontia [ORDO Disease]
- Oligodontia [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- tooth agenesis, selective, 4 [MeSH Supplementary Concept]
- tooth agenesis, selective, 4 [MeSH concept]

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