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Cowden syndrome 7
Summary
- Definition
- A Cowden syndrome that has_material_basis_in heterozygous mutation in the SEC23B gene on chromosome 20p11.
- Super Class
- Cowden syndrome
External Links
- Disease Ontology
- DOID:0081003
- Mondo Disease Ontology
- OMIM
Related Genes
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000036 | Abnormal penis morphology |
| HP:0000077 | Abnormality of the kidney |
| HP:0000130 | Abnormality of the uterus |
| HP:0000158 | Macroglossia |
| HP:0000218 | High palate |
| HP:0000221 | Furrowed tongue |
| HP:0000256 | Macrocephaly |
| HP:0000365 | Hearing impairment |
| HP:0000518 | Cataract |
| HP:0000545 | Myopia |
| Gene ID | Gene Symbol | Description |
|---|---|---|
| 5290 | PIK3CA | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha |
| 5728 | PTEN | phosphatase and tensin homolog |
| 6390 | SDHB | succinate dehydrogenase complex iron sulfur subunit B |
| 6391 | SDHC | succinate dehydrogenase complex subunit C |
| 6392 | SDHD | succinate dehydrogenase complex subunit D |
