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Congenital erythropoietic porphyria

1 OMIM reference -
2 associated genes
14 signs/symptoms

COMMON GENES: 1

Acute basophilic leukemia

2 associated genes
No signs/symptoms info

Congenital erythropoietic porphyria

Acute basophilic leukemia

GATA1	(UniProt - OMIM)		GATA1	(UniProt - OMIM)
UROS	(UniProt - OMIM)		MYB	(UniProt - OMIM)


COMMON GENES	GATA1

Citations in the biomedical literature:

Congenital erythropoietic porphyria		Acute basophilic leukemia
	Synonym(s): - CEP - GÃ¼nther disease		Synonym(s): (no synonyms)

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

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): - Neoplasms -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: variable Average age of death: adult Type of inheritance: autosomal recessive		Epidemiological data: (no data available)

	External references: 1 OMIM reference - No MeSH references		External references: No OMIM references 1 MeSH reference: D015471

Congenital erythropoietic porphyria
	Very frequent - Abnormal colour of the urine / cholic / dark urines - Auto-aggressivity / auto-mutilation - Autosomal recessive inheritance - Dental staining anomaly / spotted teeth / erythrodontia - Hemolytic anemia - Hirsutism / hypertrichosis / Increased body hair - Porphyrins metabolism anomalies / porphyria - Skin photosensitivity - Splenomegaly - Vesicles / bullous / exsudative lesions / bullous / cutaneous / mucosal detachment Frequent - Immunodeficiency / increased susceptibility to infections / recurrent infections - Mutiple fractures / bone fragility - Osteoporosis / osteopenia / demineralisation / osteomalacia / rickets Occasional - Thrombocytopenia / thrombopenia
Acute basophilic leukemia
(no data available)