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

HBB GDAP1


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


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



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

Synonym(s):
- HbSE disease

Synonym(s):
- CMT4A

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

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

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

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

No signs/symptoms info available.