Cytoscape Web
Click node...


1 OMIM reference -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
4 associated genes
No signs/symptoms info
Hereditary sensory and autonomic neuropathy type 5
Pediatric systemic lupus erythematosus

NGF IRAK1
NTRK1 PTPN22
SPP1
STAT4


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
NTRK1
(0.68)
PTPN22



Citations in the biomedical literature:


Hereditary sensory and autonomic neuropathy type 5
NGF NTRK1
Pediatric systemic lupus erythematosus
IRAK1 PTPN22 SPP1 STAT4



Hereditary sensory and autonomic neuropathy type 5
Pediatric systemic lupus erythematosus

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

Synonym(s):
- SLE, pediatric onset

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare neurologic disease
- Rare renal disease
- Rare respiratory disease
- Rare systemic or rheumatologic disease

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the musculoskeletal system and connective tissue -

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:
No OMIM references
No MeSH references

No signs/symptoms info available.