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以 HPO 交叉檢視
HPO → 對應的病歷用詞，並附加具此 HPO 的疾病作為參考。
Nephrocalcinosis
HP:0000121
對應病歷用詞(1)
- nephrocalcinosis權重 0.85已確認
具此 HPO 的疾病（附加參考）(47)
- 3-methylglutaconic aciduria-neonatal cataract-neurologic involvement-congenital neutropenia syndromeORPHA:445038 · Very frequent (99-80%)
- Distal renal tubular acidosisORPHA:18 · Very frequent (99-80%)
- Enamel-renal syndromeORPHA:1031 · Very frequent (99-80%)
- Familial isolated hyperparathyroidismORPHA:99879 · Very frequent (99-80%)
- Primary hyperoxaluria type 1ORPHA:93598 · Very frequent (99-80%)
- Primary hyperoxaluria type 2ORPHA:93599 · Very frequent (99-80%)
- Primary hyperoxaluria type 3ORPHA:93600 · Very frequent (99-80%)
- Apparent mineralocorticoid excessORPHA:320 · Frequent (79-30%)
- Autosomal dominant hypocalcemiaORPHA:428 · Frequent (79-30%)
- Beckwith-Wiedemann syndromeORPHA:116 · Frequent (79-30%)
- Blue diaper syndromeORPHA:94086 · Frequent (79-30%)
- CystinosisORPHA:213 · Frequent (79-30%)
- Dent diseaseORPHA:1652 · Frequent (79-30%)
- Generalized arterial calcification of infancyORPHA:51608 · Frequent (79-30%)
- Hyperparathyroidism-jaw tumor syndromeORPHA:99880 · Frequent (79-30%)
- Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndromeORPHA:369837 · Frequent (79-30%)
- Kidney tubulopathy-dilated cardiomyopathy syndromeORPHA:73224 · Frequent (79-30%)
- Lysinuric protein intoleranceORPHA:470 · Frequent (79-30%)
- Microvillus inclusion diseaseORPHA:2290 · Frequent (79-30%)
- Oculoskeletodental syndromeORPHA:557003 · Frequent (79-30%)
- Oncogenic osteomalaciaORPHA:352540 · Frequent (79-30%)
- Parathyroid carcinomaORPHA:143 · Frequent (79-30%)
- Primary hyperoxaluriaORPHA:416 · Frequent (79-30%)
- Primary hypomagnesemia-refractory seizures-intellectual disability syndromeORPHA:564178 · Frequent (79-30%)
- Secondary hypoparathyroidism due to impaired parathormon secretionORPHA:140286 · Frequent (79-30%)
- Trisomy 8p syndromeORPHA:264450 · Frequent (79-30%)
- X-linked hypophosphatemiaORPHA:89936 · Frequent (79-30%)
- Arthrogryposis-renal dysfunction-cholestasis syndromeORPHA:2697 · Occasional (29-5%)
- Bartter syndrome type 4ORPHA:89938 · Occasional (29-5%)
- Donohue syndromeORPHA:508 · Occasional (29-5%)
- DOORS syndromeORPHA:79500 · Occasional (29-5%)
- Familial Mediterranean feverORPHA:342 · Occasional (29-5%)
- Familial tumoral calcinosisORPHA:53715 · Occasional (29-5%)
- Fanconi-Bickel syndromeORPHA:2088 · Occasional (29-5%)
- Floating-Harbor syndromeORPHA:2044 · Occasional (29-5%)
- Glycogen storage disease due to glucose-6-phosphatase deficiency type IbORPHA:79259 · Occasional (29-5%)
- Granulomatous slack skinORPHA:33111 · Occasional (29-5%)
- HypophosphatasiaORPHA:436 · Occasional (29-5%)
- Metaphyseal chondrodysplasia, Jansen typeORPHA:33067 · Occasional (29-5%)
- Oculocerebrorenal syndrome of LoweORPHA:534 · Occasional (29-5%)
- Polyhydramnios-megalencephaly-symptomatic epilepsy syndromeORPHA:500533 · Occasional (29-5%)
- Pseudoxanthoma elasticumORPHA:758 · Occasional (29-5%)
- Rabson-Mendenhall syndromeORPHA:769 · Occasional (29-5%)
- SarcoidosisORPHA:797 · Occasional (29-5%)
- Williams syndromeORPHA:904 · Occasional (29-5%)
- Proximal renal tubular acidosisORPHA:47159 · Very rare (<4-1%)
- Familial hypocalciuric hypercalcemiaORPHA:405 · Excluded (0%)