ODCs

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1 OMIM reference -
1 associated gene
12 signs/symptoms

PROTEIN INTERACTIONS: 1

2 OMIM references -
2 associated genes
9 signs/symptoms

X-linked sideroblastic anemia - ataxia

Erythropoietic protoporphyria

ABCB7	(UniProt - OMIM)		ALAS2	(UniProt - OMIM)
			FECH	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ABCB7	(0.79)	FECH

Citations in the biomedical literature:

X-linked sideroblastic anemia - ataxia		Erythropoietic protoporphyria
	Synonym(s): (no synonyms)		Synonym(s): - EPP - XLDPP

	Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease - Rare hematologic disease - Rare neurologic disease		Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease - Rare renal disease - Rare skin disease

	Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: x-linked recessive		Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - No MeSH references		External references: 2 OMIM references - 1 MeSH reference: D046351

X-linked sideroblastic anemia - ataxia		Erythropoietic protoporphyria
	Very frequent - Anaemia - Ataxia / incoordination / trouble of the equilibrium - Nystagmus - Speech troubles / aphasia / dysphasia / echolalia / mutism / logorrhea / dysprosodia - X-linked recessive inheritance Frequent - Hypereflexia - Intellectual deficit / mental / psychomotor retardation / learning disability - Movement disorder Occasional - Hypotonia - Intrauterine growth retardation - Scoliosis - Strabismus / squint		Very frequent - Autosomal dominant inheritance - Erythema / erythematous lesions / erythroderma / polymorphous erythema - Skin photosensitivity - Urticaria Occasional - Biliary / gallbladder stones / lithiasis / cholecystitis - Cirrhosis - Cutaneous edema - Eczema - Microcytic anemia