Search Ontology:
Human Disease
Noonan syndrome 8
- Term ID
- DOID:0060586
- Synonyms
-
- NS8
- Definition
- A Noonan syndrome that has_material_basis_in caused by heterozygous mutation in the RIT1 gene on chromosome 1q22. (2)
- References
-
- ICD10CM:Q87.1
- OMIM:615355
- Ontology
- Human Disease ( DOID:0060586 )
- is a type of
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