Nephrocalcinosis

Symptom Information:

Symptom ID: HPO:0000121
Synonyms:
Nephrocalcinosis (disorder) [Orphanet:38240]
Nephrocalcinosis [Orphanet:38240]
Nephrocalcinosis [OMIM:Nephrocalcinosis]
Renal/kidney calcifications/nephrocalcinosis [Orphanet:38240]
Nephrocalcinosis [MedDRA:10029146]
Calcinosis renal [MedDRA:10029146]
Nephrocalcinosis (in some patients) [OMIM:Nephrocalcinosis (in some patients)]
Nephrocalcinosis (rare) [OMIM:Nephrocalcinosis (rare)]
Renal calcinosis [OMIM:Renal calcinosis]
Quality:
Cross references:
Orphanet:38240 "Renal/kidney calcifications/nephrocalcinosis" [Orphanet:38240]
OMIM: "Nephrocalcinosis" [OMIM:Nephrocalcinosis]
OMIM: "Nephrocalcinosis (in some patients)" [OMIM:Nephrocalcinosis (in some patients)]
OMIM: "Nephrocalcinosis (rare)" [OMIM:Nephrocalcinosis (rare)]
OMIM: "Renal calcinosis" [OMIM:Renal calcinosis]
UMLS:C0027709 "Nephrocalcinosis" [HPO:0000121]
UMLS:C0027709 "Nephrocalcinosis" [Orphanet:38240]
Is a (Direct Parents):
MedDRA Renal lithiasis
HPO         Abnormal renal morphology
Orphanet Abnormality of the urinary system physiology
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)
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)