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
R R R- R0 R1 R2 R3 R4 RA RB RC RD RE RF RG RH RI RK RM RN RO RP RQ RR RS RT RU RV RW RX RY
RE RE- REA REB REC RED REE REF REG REH REI REJ REL REM REN REO REP REQ RER RES RET REU REV REW REX

Renal glucosuria

[An autosomal inherited disorder due to defective reabsorption of GLUCOSE by the PROXIMAL RENAL TUBULES. The urinary loss of glucose can reach beyond 50 g/day. It is attributed to the mutations in the SODIUM-GLUCOSE TRANSPORTER 2 encoded by the SLC5A2 gene.(MSH)]
UMLS (ICPC) C0017980
E. Renal glucosuria; Basq. DIABETES RENALA; Da. Renal glukosuri; Du. Renale glucosurie; Finn. MUNUAISPERAINEN SOKERIVIRTSAISUUS; Fr. Glycosurie senale; G. renale Glukosurie; (108); Hung. renalis glycosuria; It. Glicosuria renale; Norw. RENAL GLYKOSURI; Port.Eu. Glicosuria de causa renal; Sp. Glucosuria renal; Sw. RENAL GLYKOSURI 
Disease or Syndrome
Relation/PAR: glycosuria; inborn renal tubular transport disorder; ENDOCRINE, METABOLIC AND NUTRITIONAL; Diagnosis/Diseases Component

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