| Metadata | |
|---|---|
| ID | DOID:0060588 |
| Name | Noonan syndrome 10 |
| Definition | A Noonan syndrome that has_material_basis_in heterozygous mutation in the LZTR1 gene on chromosome 22q11. https://www.ncbi.nlm.nih.gov/pubmed/25795793 |
| Xrefs | |
| Alternateids |
DOID:0070110 |
| Synonyms |
NS10 [EXACT] |
| Parent Relationships |
is_a autosomal dominant disease is_a Noonan syndrome |
| Subclass Logical Relationships |
has material basis in some autosomal dominant inheritance |