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1 OMIM reference -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
9 OMIM references -
9 associated genes
No signs/symptoms info
Hereditary sensory and autonomic neuropathy type 5
Zonular cataract

NGF CRYAA
NTRK1 CRYAB
CRYBA1
CRYBA4
CRYGB
CRYGC
CRYGD
HSF4
MIP


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
NGF
(0.49)
CRYAB



Citations in the biomedical literature:


Hereditary sensory and autonomic neuropathy type 5
NGF NTRK1
Zonular cataract
CRYAA CRYAB CRYBA1 CRYBA4 CRYGB CRYGC
CRYGD HSF4 MIP



Hereditary sensory and autonomic neuropathy type 5
Zonular cataract

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

Synonym(s):
- Lamellar cataract

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

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:
9 OMIM references -
1 MeSH reference: C535342

No signs/symptoms info available.