Cytoscape Web
Click node...


1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 associated gene
No signs/symptoms info
Charcot-Marie-Tooth disease type 4A
Sickle cell - hemoglobin E disease

GDAP1 HBB


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
GDAP1
(0.49)
HBB



Citations in the biomedical literature:


Charcot-Marie-Tooth disease type 4A
GDAP1
Sickle cell - hemoglobin E disease
HBB



Charcot-Marie-Tooth disease type 4A
Sickle cell - hemoglobin E disease

Synonym(s):
- CMT4A

Synonym(s):
- HbSE disease

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

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal recessive

External references:
1 OMIM reference -
1 MeSH reference: C535419
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.