Disease #02026 (CEP (porphyria, erythropoietic, congenital (CEP)), OMIM:263700)

Official abbreviation CEP
Name porphyria, erythropoietic, congenital (CEP)
OMIM ID 263700
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene UROS
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00132802 19965637-Pat3 PubMed: Bishop 2010 - M - United States white; Jewish-Ashkenazi >15y - - - CEP see paper; ... UROS UROS 1 1 Johan den Dunnen
00132803 19965637-Pat6 PubMed: Bishop 2010 - M no United States white; Jewish-Ashkenazi >20y - - - CEP see paper; required red cell transfusions , significant periods during adolescence without treatment, marked cutaneous involvement resulting from unprotected sunlight exposure UROS UROS 1 1 Johan den Dunnen
00132804 19965637-Pat10 PubMed: Bishop 2010 - M yes Switzerland Lebanon >20y - - - CEP see paper; chronic, progressive skin ulcerations since adolescence eventually disfigured sun-exposed face/hands; moderately anemic, hemoglobins ranging from 10 to 12 g/dL next decade;56y-hemoglobin 8 g/dL, red cell transfusions administered every 3w UROS UROS 1 1 Johan den Dunnen
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