Cytoscape Web
Click node...

Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Hereditary sensory and autonomic neuropathy type 5
1 OMIM reference -
2 associated genes
No signs/symptoms info
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
Hereditary sensory and autonomic neuropathy type 5

CBL
(UniProt - OMIM)
 NGF
(UniProt - OMIM)
NTRK1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
CBL
(0.72)
NTRK1


Citations in the biomedical literature:


Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
CBL
Hereditary sensory and autonomic neuropathy type 5
NGF NTRK1



Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
Hereditary sensory and autonomic neuropathy type 5

Synonym(s):
- CBL syndrome
- Noonan syndrome-like disorder with JMML
Synonym(s):
- Congenital insensitivity to pain and thermal analgesia
- HSAN5
- NHSA5
Classification (Orphanet):
- Rare cardiac disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: D000699
No signs/symptoms info available.