Nephrocalcinosis
Symptom Information:
Symptom ID: | HPO:0000121 | |||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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 upper urinary tract(HPO:0010935) Abnormality of the kidney(HPO:0000077) Abnormal renal morphology(HPO:0012210) Nephrocalcinosis(HPO:0000121) MedDRA: Renal and urinary disorders(MedDRA:10038359) Nephrolithiasis(HPO:0000787) Renal lithiasis(MedDRA:10038478) Nephrocalcinosis(HPO:0000121) |
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Database Frequency: | 57 / 7739 | |||||||||
Resource: |
All diseases associated with this symptom:
ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 2 | (OMIM:614473) |
ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2 | (OMIM:613404) |
Alport syndrome | (Orphanet:63) |
Alström syndrome | (Orphanet:64) |
Amelogenesis imperfecta - nephrocalcinosis | (Orphanet:1031) |
Arthrogryposis - renal dysfunction - cholestasis | (Orphanet:2697) |
Autosomal dominant distal renal tubular acidosis | (Orphanet:93608) |
Autosomal recessive distal renal tubular acidosis without deafness | (Orphanet:93609) |
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) |
Blue diaper syndrome | (Orphanet:94086) |
Congenital sucrase-isomaltase deficiency | (Orphanet:35122) |
Cystinosis | (Orphanet:213) |
Dent disease type 1 | (Orphanet:93622) |
Dent disease type 2 | (Orphanet:93623) |
Distal renal tubular acidosis | (Orphanet:18) |
Distal renal tubular acidosis with anemia | (Orphanet:93610) |
FANCONI RENOTUBULAR SYNDROME 4 WITH MATURITY-ONSET DIABETES OF THEYOUNG | (OMIM:616026) |
Familial Mediterranean fever | (Orphanet:342) |
Familial hypomagnesemia - hypercalciuria - nephrocalcinosis | (Orphanet:31043) |
Familial hypomagnesemia - hypercalciuria - nephrocalcinosis - severe ocular involvement | (Orphanet:2196) |
Floating-Harbor syndrome | (Orphanet:2044) |
Glycogen storage disease due to glucose-6-phosphatase deficiency type a | (Orphanet:79258) |
Glycogen storage disease due to glucose-6-phosphatase deficiency type b | (Orphanet:79259) |
HYPERPARATHYROIDISM, NEONATAL SELF-LIMITED PRIMARY, WITH HYPERCALCIURIA | (OMIM:239199) |
HYPOPHOSPHATEMIC RICKETS, X-LINKED RECESSIVE | (OMIM:300554) |
Hypercalcemic tumoral calcinosis | (Orphanet:306661) |
Hypophosphatemic rickets, autosomal recessive, 2 | (OMIM:613312) |
Infantile hypophosphatasia | (Orphanet:247651) |
Intellectual disability-seizures-hypotonia-ophthalmologic-skeletal anomalies syndrome | (Orphanet:369837) |
Metaphyseal chondrodysplasia, Jansen type | (Orphanet:33067) |
NEPHROLITHIASIS, X-LINKED RECESSIVE, WITH RENAL FAILURE | (OMIM:310468) |
Navajo neurohepatopathy | (Orphanet:255229) |
Neonatal severe primary hyperparathyroidism | (Orphanet:417) |
Oculocerebrorenal syndrome | (Orphanet:534) |
POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY | (OMIM:611087) |
PROTEINURIA, LOW MOLECULAR WEIGHT, WITH HYPERCALCIURIA AND NEPHROCALCINOSIS | (OMIM:308990) |
Perinatal lethal hypophosphatasia | (Orphanet:247623) |
Primary Fanconi syndrome | (Orphanet:3337) |
Primary hyperoxaluria | (Orphanet:416) |
Primary hyperoxaluria type 1 | (Orphanet:93598) |
Primary hyperoxaluria type 2 | (Orphanet:93599) |
Pseudoxanthoma elasticum | (Orphanet:758) |
RENAL TUBULAR ACIDOSIS III | (OMIM:267200) |
SIDEROBLASTIC ANEMIA WITH B-CELL IMMUNODEFICIENCY, PERIODIC FEVERS,AND DEVELOPMENTAL DELAY | (OMIM:616084) |
Short-rib thoracic dysplasia 11 with or without polydactyly | (OMIM:615633) |
Shwachman-Diamond syndrome | (Orphanet:811) |
Tumoral calcinosis | (Orphanet:53715) |
Tyrosinemia type 1 | (Orphanet:882) |
Williams syndrome | (Orphanet:904) |
Wilson disease | (Orphanet:905) |
[DEL] ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1 | (OMIM:208085) |
[DEL] GLYCOGEN STORAGE DISEASE Ib | (OMIM:232220) |