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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
H H+ H1 HA HB HC HD HE HF HG HH HI HK HL HM HN HO HP HQ HR HS HT HU HV HX HY HZ
HEA HEB HEC HED HEE HEF HEI HEL HEM HEN HEP HER HES HET HEU HEV HEX HEY

Hereditary hemolytic anemias

[includes hereditary erythrocyte membrane defects, enzyme deficiencies, hemoglobin abnormalities, stem cell defects (paroxysmal nocturnal hemoglobinuria), and alloimmune (Rh) disease of newborn.(CSP)]
UMLS (ICPC) C0002881
E. Hereditary hemolytic anemias; Basq. ANEMIA HEMOLITIKOA; Da. Medfodt haemolytisk anaemi; Du. Erfelijke hemolytische anemie; Finn. PERINNOLLISET HEMOLYYTTISET ANEMIAT; Fr. Anemies hemolytiques hereditaires; G. Hereditaere Haemolytische Anaemie; (108); Hung. orokletes haemolytikus anaemiak; It. Anemie emolitiche ereditarie; Norw. MEDFODTE HEMOLYTISKE ANEMIER; Port.Eu. Anemias hemoliticas hereditarias; Sp. Anemias hemoliticas hereditarias; Sw. ARFTLIGA HEMOLYTISKA ANEMIER 
Disease or Syndrome

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