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Hereditary sensory and autonomic neuropathy type 5
1 OMIM reference -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
2 OMIM references -
3 associated genes
No signs/symptoms info
Hereditary sensory and autonomic neuropathy type 5
Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes

NGF
(UniProt - OMIM)
 NPHS1
(UniProt - OMIM)
NTRK1
(UniProt - OMIM)
 NPHS2
(UniProt - OMIM)
PTPRO
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
NTRK1
(0.68)
PTPRO


Citations in the biomedical literature:


Hereditary sensory and autonomic neuropathy type 5
NGF NTRK1
Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
NPHS1 NPHS2 PTPRO



Hereditary sensory and autonomic neuropathy type 5
Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes

Synonym(s):
- Congenital insensitivity to pain and thermal analgesia
- HSAN5
- NHSA5
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the genitourinary system -
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:
2 OMIM references -
No MeSH references
No signs/symptoms info available.