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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。
Hypophosphatemia
HP:0002148
對應病歷用詞(3)
- low phosphate權重 0.9已確認
- 低血磷權重 0.9已確認
- 血磷過低權重 0.85已確認
具此 HPO 的疾病（附加參考）(24)
- Autosomal dominant hypophosphatemic ricketsORPHA:89937 · Very frequent (99-80%)
- CystinosisORPHA:213 · Very frequent (99-80%)
- Familial isolated hyperparathyroidismORPHA:99879 · Very frequent (99-80%)
- Fanconi-Bickel syndromeORPHA:2088 · Very frequent (99-80%)
- Hereditary hypophosphatemic rickets with hypercalciuriaORPHA:157215 · Very frequent (99-80%)
- Hyperparathyroidism-jaw tumor syndromeORPHA:99880 · Very frequent (99-80%)
- Hypocalcemic vitamin D-dependent ricketsORPHA:289157 · Very frequent (99-80%)
- Hypocalcemic vitamin D-resistant ricketsORPHA:93160 · Very frequent (99-80%)
- Infantile nephropathic cystinosisORPHA:411629 · Very frequent (99-80%)
- Oncogenic osteomalaciaORPHA:352540 · Very frequent (99-80%)
- Parathyroid carcinomaORPHA:143 · Very frequent (99-80%)
- X-linked hypophosphatemiaORPHA:89936 · Very frequent (99-80%)
- Colchicine poisoningORPHA:31824 · Frequent (79-30%)
- Fibrous dysplasia of boneORPHA:249 · Frequent (79-30%)
- Metaphyseal chondrodysplasia, Jansen typeORPHA:33067 · Frequent (79-30%)
- Primary Fanconi renotubular syndromeORPHA:3337 · Frequent (79-30%)
- Autosomal recessive malignant osteopetrosisORPHA:667 · Occasional (29-5%)
- Hereditary fructose intoleranceORPHA:469 · Occasional (29-5%)
- Juvenile nephropathic cystinosisORPHA:411634 · Occasional (29-5%)
- Linear verrucous nevus syndromeORPHA:2611 · Occasional (29-5%)
- Oculocerebrorenal syndrome of LoweORPHA:534 · Occasional (29-5%)
- Pearson syndromeORPHA:699 · Occasional (29-5%)
- Refractory celiac diseaseORPHA:398063 · Occasional (29-5%)
- McCune-Albright syndromeORPHA:562 · Very rare (<4-1%)