ODCs

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1 OMIM reference -
1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

Autosomal dominant Charcot-Marie-Tooth disease type 2K

Sickle cell anemia


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

Citations in the biomedical literature:

Autosomal dominant Charcot-Marie-Tooth disease type 2K		Sickle cell anemia
	Synonym(s): - CMT2K		Synonym(s): - Sickle cell disease

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare bone disease - Rare endocrine disease - Rare genetic disease - Rare gynecologic or obstetric disease - Rare hematologic disease - Rare infertility - Rare renal 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: <1 / 1 000 000 Average age onset: adolescence / young Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: 1-5 / 10 000 Average age onset: variable Average age of death: adult Type of inheritance: autosomal recessive

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: D000755

No signs/symptoms info available.