Autosomal dominant hypocalcemia
|
(Orphanet:428)
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Autosomal recessive infantile hypercalcemia
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(Orphanet:300547)
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BARTTER SYNDROME, ANTENATAL, TYPE 1
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(OMIM:601678)
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BARTTER SYNDROME, ANTENATAL, TYPE 2
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(OMIM:241200)
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Bartter syndrome
|
(Orphanet:112)
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Bartter syndrome with hypocalcemia
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(Orphanet:263417)
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Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11
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(Orphanet:96193)
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Cystic fibrosis
|
(Orphanet:586)
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Cystic fibrosis - gastritis - megaloblastic anemia
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(Orphanet:2575)
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Cystinuria type A
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(Orphanet:93612)
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Cystinuria type B
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(Orphanet:93613)
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Dent disease type 1
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(Orphanet:93622)
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Dent disease type 2
|
(Orphanet:93623)
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Dominant hypophosphatemia with nephrolithiasis or osteoporosis
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(Orphanet:244305)
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FANCONI RENOTUBULAR SYNDROME 2
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(OMIM:613388)
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Familial hyperaldosteronism type 3
|
(Orphanet:251274)
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Familial hypomagnesemia - hypercalciuria - nephrocalcinosis
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(Orphanet:31043)
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Familial hypomagnesemia - hypercalciuria - nephrocalcinosis - severe ocular involvement
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(Orphanet:2196)
|
HYPERCALCIURIA, ABSORPTIVE, 2
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(OMIM:143870)
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HYPERPARATHYROIDISM, NEONATAL SELF-LIMITED PRIMARY, WITH HYPERCALCIURIA
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(OMIM:239199)
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HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE
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(OMIM:300554)
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HYPOURICEMIA, HYPERCALCINURIA, AND DECREASED BONE DENSITY
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(OMIM:242050)
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Hereditary hypophosphatemic rickets with hypercalciuria
|
(Orphanet:157215)
|
IMAGe syndrome
|
(Orphanet:85173)
|
Idiopathic hypercalciuria
|
(Orphanet:2197)
|
Infantile hypophosphatasia
|
(Orphanet:247651)
|
Intellectual disability-seizures-hypotonia-ophthalmologic-skeletal anomalies syndrome
|
(Orphanet:369837)
|
MELAS
|
(Orphanet:550)
|
MOVED TO 614732
|
(OMIM:300290)
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Medullary sponge kidney
|
(Orphanet:1309)
|
Metaphyseal chondrodysplasia, Jansen type
|
(Orphanet:33067)
|
NEPHROLITHIASIS, X-LINKED RECESSIVE, WITH RENAL FAILURE
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(OMIM:310468)
|
NEPHROLITHIASIS/OSTEOPOROSIS, HYPOPHOSPHATEMIC, 1
|
(OMIM:612286)
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Neonatal severe primary hyperparathyroidism
|
(Orphanet:417)
|
Oculocerebrorenal syndrome
|
(Orphanet:534)
|
PROTEINURIA, LOW MOLECULAR WEIGHT, WITH HYPERCALCIURIA AND NEPHROCALCINOSIS
|
(OMIM:308990)
|
Perinatal lethal hypophosphatasia
|
(Orphanet:247623)
|
Primary Fanconi syndrome
|
(Orphanet:3337)
|
Primary hyperoxaluria type 3
|
(Orphanet:93600)
|
SARCOIDOSIS, SUSCEPTIBILITY TO, 1
|
(OMIM:181000)
|
Sarcoidosis
|
(Orphanet:797)
|
Tubular renal disease-cardiomyopathy syndrome
|
(Orphanet:73224)
|
Tyrosinemia type 1
|
(Orphanet:882)
|
Williams syndrome
|
(Orphanet:904)
|
Wilson disease
|
(Orphanet:905)
|