Hypercalciuria

Symptom Information:

Symptom ID: HPO:0002150
Synonyms:
Hypercalcinuria [HPO:0002150]
Hypercalciuria (disorder) [Orphanet:49260]
Hypercalciuria [Orphanet:49260]
Hypercalcinuria [OMIM:Hypercalcinuria]
Hypercalciuria [OMIM:Hypercalciuria]
Hypercalciuria [MedDRA:10020590]
Calcium crystalluria [MedDRA:10020590]
Crystalluria calcium [MedDRA:10020590]
Hypercalcinuria [MedDRA:10020590]
Idiopathic hypercalciuria [MedDRA:10020590]
Hypercalciuria (in childhood) [OMIM:Hypercalciuria (in childhood)]
Quality:
Cross references:
Orphanet:49260 "Hypercalciuria" [Orphanet:49260]
OMIM: "Hypercalcinuria" [OMIM:Hypercalcinuria]
OMIM: "Hypercalciuria" [OMIM:Hypercalciuria]
OMIM: "Hypercalciuria (in childhood)" [OMIM:Hypercalciuria (in childhood)]
UMLS:C0020438 "Hypercalciuria" [HPO:0002150]
UMLS:C0020438 "Hypercalciuria" [Orphanet:49260]
Is a (Direct Parents):
Orphanet Abnormality of calcium-phosphate metabolism
MedDRA Hyperparathyroid disorders
HPO         Abnormality of calcium homeostasis
HPO         Abnormality of urine calcium concentration
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the genitourinary system(HPO:0000119)
          Abnormality of the urinary system(HPO:0000079)
             Abnormality of the urinary system physiology(HPO:0011277)
                Abnormality of urine homeostasis(HPO:0003110)
                   Abnormal urinary electrolyte concentration(HPO:0012591)
                      Abnormality of urine calcium concentration(HPO:0011280)
                         Hypercalciuria(HPO:0002150)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Abnormality of ion homeostasis(HPO:0003111)
             Abnormality of cation homeostasis(HPO:0010929)
                Abnormality of divalent inorganic cation homeostasis(HPO:0010927)
                   Abnormality of calcium homeostasis(HPO:0004363)
                      Hypercalciuria(HPO:0002150)
          Abnormality of urine homeostasis(HPO:0003110)
             Abnormal urinary electrolyte concentration(HPO:0012591)
                Abnormality of urine calcium concentration(HPO:0011280)
                   Hypercalciuria(HPO:0002150)
MedDRA:
Endocrine disorders(MedDRA:10014698)
    Parathyroid gland disorders(MedDRA:10033949)
       Hyperparathyroid disorders(MedDRA:10020704)
          Hypercalciuria(HPO:0002150)
Database Frequency: 45 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant hypocalcemia (Orphanet:428)
Autosomal recessive infantile hypercalcemia (Orphanet:300547)
BARTTER SYNDROME, ANTENATAL, TYPE 1 (OMIM:601678)
BARTTER SYNDROME, ANTENATAL, TYPE 2 (OMIM:241200)
Bartter syndrome (Orphanet:112)
Bartter syndrome with hypocalcemia (Orphanet:263417)
Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11 (Orphanet:96193)
Cystic fibrosis (Orphanet:586)
Cystic fibrosis - gastritis - megaloblastic anemia (Orphanet:2575)
Cystinuria type A (Orphanet:93612)
Cystinuria type B (Orphanet:93613)
Dent disease type 1 (Orphanet:93622)
Dent disease type 2 (Orphanet:93623)
Dominant hypophosphatemia with nephrolithiasis or osteoporosis (Orphanet:244305)
FANCONI RENOTUBULAR SYNDROME 2 (OMIM:613388)
Familial hyperaldosteronism type 3 (Orphanet:251274)
Familial hypomagnesemia - hypercalciuria - nephrocalcinosis (Orphanet:31043)
Familial hypomagnesemia - hypercalciuria - nephrocalcinosis - severe ocular involvement (Orphanet:2196)
HYPERCALCIURIA, ABSORPTIVE, 2 (OMIM:143870)
HYPERPARATHYROIDISM, NEONATAL SELF-LIMITED PRIMARY, WITH HYPERCALCIURIA (OMIM:239199)
HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE (OMIM:300554)
HYPOURICEMIA, HYPERCALCINURIA, AND DECREASED BONE DENSITY (OMIM:242050)
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)
Medullary sponge kidney (Orphanet:1309)
Metaphyseal chondrodysplasia, Jansen type (Orphanet:33067)
NEPHROLITHIASIS, X-LINKED RECESSIVE, WITH RENAL FAILURE (OMIM:310468)
NEPHROLITHIASIS/OSTEOPOROSIS, HYPOPHOSPHATEMIC, 1 (OMIM:612286)
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)