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531:Mitochondrial pyruvate carrier deficiency
426:Recessive multiple epiphyseal dysplasia
189:Congenital endothelial dystrophy type 2
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568:table with the collapsible attribute
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236:Thyroid dyshormonogenesis type 1
413:Multiple epiphyseal dysplasia 4
208:Glucose-galactose malabsorption
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345:Allan–Herndon–Dudley syndrome
264:Lysinuric protein intolerance
493:Acrodermatitis enteropathica
143:Arterial tortuosity syndrome
175:Hereditary elliptocytosis 4
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171:Hereditary spherocytosis 4
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431:Atelosteogenesis, type II
613:Solute carrier disorders
589:Solute carrier disorders
115:Fanconi-Bickel syndrome
129:Fructose malabsorption
545:solute carrier family
507:African iron overload
436:Diastrophic dysplasia
478:Von Gierke's disease
359:Von Gierke's disease
194:Fuchs' dystrophy 4
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317:Gitelman syndrome
73:Episodic ataxia 6
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47:Genetic disorder
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278:Cystinuria
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600:collapsed
578:parameter
543:see also
53:disorders
637:Category
624:expanded
480:, GSD-Ib
361:, GSD-Ic
526:SLC54A1
501:SLC40A1
487:SLC39A4
472:SLC37A4
464:CDOG 2C
458:SLC35C1
444:SLC26A4
421:type 1B
407:SLC26A2
382:SLC17A8
368:SLC17A5
353:SLC17A3
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325:SLC16A1
311:SLC12A3
297:SLC11A1
244:SLC6A19
183:SLC4A11
137:SLC2A10
87:SPATCCM
388:DFNA25
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258:SLC7A7
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619:state
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331:HHF7
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