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1 OMIM reference -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 2
1 OMIM reference -
5 associated genes
No signs/symptoms info
Hereditary sensory and autonomic neuropathy type 5
Juvenile myelomonocytic leukemia

NGF CBL
NTRK1 KRAS
NF1
NRAS
PTPN11


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
NTRK1
NTRK1
(0.72)
(0.52)
CBL
PTPN11



Citations in the biomedical literature:


Hereditary sensory and autonomic neuropathy type 5
NGF NTRK1
Juvenile myelomonocytic leukemia
CBL KRAS NF1 NRAS PTPN11



Hereditary sensory and autonomic neuropathy type 5
Juvenile myelomonocytic leukemia

Synonym(s):
- Congenital insensitivity to pain and thermal analgesia
- HSAN5
- NHSA5

Synonym(s):
- Juvenile chronic myelomonocytic leukemia

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Neoplasms -

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
(no data available)

External references:
1 OMIM reference -
1 MeSH reference: D000699
External references:
1 OMIM reference -
1 MeSH reference: D054429

No signs/symptoms info available.