Hereditary kidney diseases
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Congenital abnormalities of the kidney and urinary tract
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Cystic kidney disease
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Disorders of tubular solute transport
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Hereditary glomerular disease
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Hereditary metabolic kidney disease
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Hereditary renal tumors
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Interstitial kidney disease
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Kidney disease appearing as endocrinological disorders
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Thrombotic microangiopathies
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Urolithiasis
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Cystinuria
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SLC3A1
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SLC7A9
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Dicarboxylic aminoaciduria
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SLC1A1
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Dihydroxyadenin urolithiasis
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APRT
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Nephrocalcinosis
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Bartter syndrome
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Antenatal Bartter syndrome type 1
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SLC12A1
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Antenatal Bartter syndrome type 2
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KCNJ1
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Classic Bartter syndrome
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CLCNKB
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Hypercalciuric hypocalcemia 1
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CASR
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Hypercalciuric hypocalcemia 2
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GNA11
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Infantile Bartter syndrome with deafness type 4
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BSND
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CLCNKA
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CLCNKB
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Transient antenatal Bartter syndrome
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MAGED2
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Dent disease
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CLCN5
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OCRL
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Hereditary Rickets
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Hypophosphatasia
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Adult hypophosphatasia
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ALPL
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Childhood hypophosphatasia
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ALPL
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Infantile hypophosphatasia
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ALPL
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Odontohypophosphatasia
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ALPL
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Hypophosphatemic bone and kindney disease
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Disorders of the renal phosphate transporters
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Hypophosphatemic rickets with hypercalciuria
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SLC34A3
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Idiopathic basal ganglia calcification 1
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SLC20A2
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Nephrolithiasis/osteoporosis, hypophosphatemic, 1
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SLC34A1
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Nephrolithiasis/osteoporosis, hypophosphatemic, 2
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SLC9A3R1
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FGF23-induced hypophosphatemic rickets
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Autosomal dominant hypophosphatemic rickets
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FGF23
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Autosomal recessive hypophosphatemic rickets type 1
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DMP1
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Autosomal recessive hypophosphatemic rickets type 2
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ENPP1
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X-linked dominant hypophosphatemic rickets
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PHEX
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Fanconi-type hypophosphatemic rickets
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Nephrolithiasis/osteoporosis, hypophosphatemic, 1
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SLC34A1
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X-linked recessive hypophosphatemic rickets
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CLCN5
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OCRL
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Hypophosphatemic rickets with hyperparathyroidism
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KL
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Osteoglophonic dysplasia
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FGFR1
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Raine syndrome
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FAM20C
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X-linked dominant hypophosphatemic rickets
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PHEX
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Vitamin D hydroxylation-deficient rickets type 1A
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CYP27B1
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Vitamin D hydroxylation-deficient rickets type 1B
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CYP2R1
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Vitamin D-dependent rickets, type 2A
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VDR
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Vitamin D-dependent rickets, type 2B
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RXRA
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Hyperoxaluria
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Hyperoxaluria type 1
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AGXT
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Hyperoxaluria type 2
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GRHPR
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Hyperoxaluria type 3
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HOGA1
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Hypomagnesemia with hypercalciuria and nephrocalcinosis
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CLDN16
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Hypomagnesemia with hypercalciuria and nephrocalcinosis with ocular involvement
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CLDN19
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Infantile hypercalcemia
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CYP24A1
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Lowe disease
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OCRL
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Renal tubular acidosis
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Combined renal tubular acidosis 3 with osteopetrosis 3
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CA2
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Distal renal tubular acidosis (autosomal dominant)
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SLC4A1
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Distal renal tubular acidosis (autosomal recessive)
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ATP6V0A4
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Distal renal tubular acidosis with deafness (autosomal recessive)
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ATP6V1B1
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Proximal renal tubular acidosis
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SLC4A4
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Renal tubular acidosis with arthrogryposis
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Arthrogryposis, renal dysfunction, and cholestasis 1
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VPS33B
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Arthrogryposis, renal dysfunction, and cholestasis 2
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VIPAS39
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Williams-Beuren syndrome
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ELN
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Nephrolithiasis diarrhea syndrome
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SLC26A6
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Susceptibility to nephrolithiasis
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ALPL
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CASR
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SLC26A1
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TRPV5
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ZNF365
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Uric acid nephropathy
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Hyperuricemic nephropathy
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Hyperuricemic nephropathy, familial juvenile 1
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UMOD
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Hyperuricemic nephropathy, familial juvenile 2
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REN
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Kelley-Seegmiller syndrome
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HPRT1
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Lesch-Nyhan syndrome
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HPRT1
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Renal Hypouricemia
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SLC22A12
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SLC2A9
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