UMLS. CSP-HL7-ICD9CM-NCI-NDFRT-RXNORM
%
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
E E0 E6 E7 EA EB EC ED EE EF EG EH EI EJ EK EL EM EN EO EP EQ ER ES ET EU EV EW EX EY
EP- EP4 EPA EPE EPH EPI EPM EPN EPO EPP EPR EPS EPT

EPP (erythropoietic protoporphyria porphyria)

[autosomal dominant disorder due to partial deficiency of ferrochelatase, characterized by an excess of protoporphyrin and a wide variety of photosensitive skin changes. ( CSP )]
UMLS (CSP) C0162568
 
Disease or Syndrome
Relation/PAR: Genetic Condition
DIS PORPHYRIN METABOLISM

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