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1 OMIM reference -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Hereditary sensory and autonomic neuropathy type 5
Feingold syndrome type 1

NGF MYCN
NTRK1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
NTRK1
(0.63)
MYCN



Citations in the biomedical literature:


Hereditary sensory and autonomic neuropathy type 5
NGF NTRK1
Feingold syndrome type 1
MYCN



Hereditary sensory and autonomic neuropathy type 5
Feingold syndrome type 1

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

Synonym(s):
- Brunner-Winter syndrome type 1
- Digital anomalies with short palpebral fissures and atresia of esophagus or duodenum type 1
- FGLDS1
- FS1
- MMT type 1
- MODED syndrome type 1
- Microcephaly - intellectual deficit - tracheoesophageal fistula type 1
- Microcephaly - oculo-digito-esophageal-duodenal syndrome type 1
- Microcephaly-digital anomalies-normal intelligence type 1
- ODED syndrome type 1
- Oculo-digito-esophageal-duodenal syndrome type 1

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare abdominal surgical disease
- Rare bone disease
- Rare developmental defect during embryogenesis
- 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:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: adult
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
1 MeSH reference: D000699
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.