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Noonan syndrome 6
Summary
- Synonym
-
- NS6
- Definition
- A Noonan syndrome that has_material_basis_in heterozygous mutation in the NRAS gene on chromosome 1p13.
- Super Class
- Noonan syndrome autosomal dominant disease
External Links
- Disease Ontology
- DOID:0060584
- Mondo Disease Ontology
- MeSH
- OMIM
Related Genes
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000347 | Micrognathia |
| HP:0000486 | Strabismus |
| HP:0000179 | Thick lower lip vermilion |
| HP:0000407 | Sensorineural hearing impairment |
| HP:0000044 | Hypogonadotropic hypogonadism |
| HP:0000368 | Low-set, posteriorly rotated ears |
| HP:0000474 | Thickened nuchal skin fold |
| HP:0000316 | Hypertelorism |
| HP:0000028 | Cryptorchidism |
| HP:0000391 | Thickened helices |
