tooth agenesis, selective, 9
MONDO:0014999Mondo
Findings
No curated finding names tooth agenesis, selective, 9 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any tooth agenesis in which the cause of the disease is a mutation in the GREM2 gene.
Definition from the Mondo Disease Ontology (MONDO:0014999), read 2026-09-29. CC BY 4.0.
- Inheritance
- Autosomal dominant inheritance
HPO, annotations 2026-09-02
Features
3 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Selective tooth agenesisHPOHP:0001592
- 6 of 7 reported patients
- MicrodontiaHPOHP:0000691
- 1 of 7 reported patients
- TaurodontiaHPOHP:0000679
- 1 of 7 reported patients
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- GREM2HGNC:17655
- Limited · ClinGen · Autosomal dominant · 2025
Where it sits
- A kind of
Other names
5 names
Resolves to: tooth agenesis, selective, 9
- Also called
- GREM2 tooth agenesisSTHAG9tooth agenesis caused by mutation in GREM2tooth agenesis, selective, 9; STHAG9tooth agenesis, selective, type 9