Disease #00724 (NFNS (neurofibromatosis-Noonan syndrome (NFNS)), OMIM:601321)
Official abbreviation |
NFNS |
Name |
neurofibromatosis-Noonan syndrome (NFNS) |
OMIM ID |
601321 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
NF1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
|