Tooth agenesis, selective, 1

Synonyms: HYPODONTIA/OLIGODONTIA 1; SECOND PREMOLARS AND THIRD MOLARS, ABSENCE OF

Summary

Any tooth agenesis in which the cause of the disease is a mutation in the MSX1 gene characterized by varying severity of tooth agenesis that may be seen in combination with orofacial clefting in some individuals. [from MONDO]

Available tests

15 tests are in the database for this condition.

Clinical tests (15 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

Associated genes Help
Genes reported to contribute to the condition.

MSX1
60 tests
Also known as: ECTD3, HOX7, HYD1, STHAG1, MSX1
Summary: msh homeobox 1

Imported from Human Phenotype Ontology (HPO)

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Abnormality of head or neck
- Partial congenital absence of teeth
  Partial congenital absence of teeth
  - MedGen UID: 43794
  - Concept ID: C0020608
  - Finding: Congenital Abnormality
  Abnormality of head or neck
  See: Feature record | Search on this feature

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