Alström syndrome
|
(Orphanet:64)
|
Arthrogryposis - renal dysfunction - cholestasis
|
(Orphanet:2697)
|
BILIARY MALFORMATION WITH RENAL TUBULAR INSUFFICIENCY
|
(OMIM:210550)
|
Bardet-Biedl syndrome 12
|
(OMIM:615989)
|
CYSTINOSIS, NEPHROPATHIC
|
(OMIM:219800)
|
Cystinosis
|
(Orphanet:213)
|
Dent disease type 1
|
(Orphanet:93622)
|
Dent disease type 2
|
(Orphanet:93623)
|
FANCONI RENOTUBULAR SYNDROME 2
|
(OMIM:613388)
|
FANCONI RENOTUBULAR SYNDROME 3
|
(OMIM:615605)
|
FANCONI RENOTUBULAR SYNDROME 4 WITH MATURITY-ONSET DIABETES OF THEYOUNG
|
(OMIM:616026)
|
Fabry disease
|
(Orphanet:324)
|
Fanconi renotubular syndrome 1
|
(OMIM:134600)
|
GLUCOGLYCINURIA
|
(OMIM:138070)
|
Glucose-galactose malabsorption
|
(Orphanet:35710)
|
Glycogen storage disease due to GLUT2 deficiency
|
(Orphanet:2088)
|
Hemochromatosis, type 2A
|
(OMIM:602390)
|
Hereditary fructose intolerance
|
(Orphanet:469)
|
INTERSTITIAL NEPHRITIS, KARYOMEGALIC
|
(OMIM:614817)
|
Isolated cytochrome C oxidase deficiency
|
(Orphanet:254905)
|
Juvenile cataract - microcornea - renal glucosuria
|
(Orphanet:247794)
|
Maturity-onset diabetes of the young, type 3
|
(OMIM:600496)
|
Multiple acyl-CoA dehydrogenase deficiency
|
(Orphanet:26791)
|
PROTEINURIA, LOW MOLECULAR WEIGHT, WITH HYPERCALCIURIA AND NEPHROCALCINOSIS
|
(OMIM:308990)
|
Pancreatic hypoplasia - diabetes - congenital heart disease
|
(Orphanet:2255)
|
Pearson syndrome
|
(Orphanet:699)
|
Primary Fanconi syndrome
|
(Orphanet:3337)
|
Rabson-Mendenhall syndrome
|
(Orphanet:769)
|
Renal cysts and diabetes syndrome
|
(Orphanet:93111)
|
Renal glucosuria
|
(Orphanet:69076)
|
Tyrosinemia type 1
|
(Orphanet:882)
|
Wilson disease
|
(Orphanet:905)
|