Input | HPO ID | HPO term | Distance | Gene | Gene id entrez | HGNC ID | DiseaseId | DiseaseName | Frequency | Onset | HGMD variants | ClinVar variants |
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HPO disease - gene - phenotype typical associations: |
HPO disease - gene - phenotype less frequent non-typical associations: |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | ABCC6 CL E G H | 368 | 57 | OMIM:614473 | Arterial calcification, generalized, of infancy, 2 | | | | 415 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | ABCC6 CL E G H | 368 | 57 | ORPHA:51608 | Generalized arterial calcification of infancy | | | | 415 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | ALDOB CL E G H | 229 | 417 | OMIM:229600 | Fructose intolerance, hereditary | . | | | 73 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | ALDOB CL E G H | 229 | 417 | ORPHA:469 | Hereditary fructose intolerance | HP:0040283 - Occasional | | | 73 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | AP2S1 CL E G H | 1175 | 565 | OMIM:600740 | Hypocalciuric hypercalcemia, familial, type III | . | | | 6 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | CACNA1S CL E G H | 779 | 1397 | ORPHA:79102 | Thyrotoxic periodic paralysis | | | | 247 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | CASR CL E G H | 846 | 1514 | OMIM:239200 | Hyperparathyroidism, neonatal severe | . | | | 272 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | CDC73 CL E G H | 79577 | 16783 | ORPHA:99879 | Familial isolated hyperparathyroidism | HP:0040281 - Very frequent | | | 169 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | CDC73 CL E G H | 79577 | 16783 | ORPHA:99880 | Hyperparathyroidism-jaw tumor syndrome | HP:0040281 - Very frequent | | | 169 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | CDC73 CL E G H | 79577 | 16783 | ORPHA:143 | Parathyroid carcinoma | HP:0040281 - Very frequent | | | 169 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | CLCN5 CL E G H | 1184 | 2023 | OMIM:300009 | Dent disease 1 | . | | | 112 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | CLCN5 CL E G H | 1184 | 2023 | OMIM:300554 | Hypophosphatemic rickets, X-linked recessive | . | | | 112 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | CLCN5 CL E G H | 1184 | 2023 | OMIM:308990 | Proteinuria, low molecular weight, with hypercalciuric nephrocalcinosis | . | | | 112 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | CLCN7 CL E G H | 1186 | 2025 | ORPHA:667 | Autosomal recessive malignant osteopetrosis | HP:0040283 - Occasional | | | 102 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | COL4A3 CL E G H | 1285 | 2204 | OMIM:104200 | Alport syndrome, autosomal dominant | . | | | 161 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | CTNS CL E G H | 1497 | 2518 | OMIM:219800 | Cystinosis, nephropathic | | | | 178 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | CTNS CL E G H | 1497 | 2518 | ORPHA:411629 | Infantile nephropathic cystinosis | HP:0040281 - Very frequent | | | 178 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | CTNS CL E G H | 1497 | 2518 | ORPHA:411634 | Juvenile nephropathic cystinosis | HP:0040283 - Occasional | | | 178 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | CYP27B1 CL E G H | 1594 | 2606 | ORPHA:289157 | Hypocalcemic vitamin D-dependent rickets | HP:0040281 - Very frequent | | | 41 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | CYP27B1 CL E G H | 1594 | 2606 | OMIM:264700 | Vitamin D hydroxylation-deficient rickets, type 1A | . | | | 41 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | CYP2R1 CL E G H | 120227 | 20580 | ORPHA:289157 | Hypocalcemic vitamin D-dependent rickets | HP:0040281 - Very frequent | | | 5 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | CYP2R1 CL E G H | 120227 | 20580 | OMIM:600081 | Vitamin D hydroxylation-deficient rickets, type 1B | . | | | 5 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | CYP3A4 CL E G H | 1576 | 2637 | OMIM:619073 | VITAMIN D-DEPENDENT RICKETS, TYPE 3; VDDR3 | | | | 2 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | DMP1 CL E G H | 1758 | 2932 | ORPHA:289176 | Autosomal recessive hypophosphatemic rickets | | | | 48 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | DMP1 CL E G H | 1758 | 2932 | OMIM:241520 | Hypophosphatemic rickets, autosomal recessive | . | | | 48 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | EHHADH CL E G H | 1962 | 3247 | ORPHA:3337 | Primary Fanconi renotubular syndrome | HP:0040282 - Frequent | | | 2 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | ENPP1 CL E G H | 5167 | 3356 | OMIM:208000 | Arterial calcification, generalized, of infancy, 1 | | | | 151 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | ENPP1 CL E G H | 5167 | 3356 | ORPHA:289176 | Autosomal recessive hypophosphatemic rickets | | | | 151 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | ENPP1 CL E G H | 5167 | 3356 | ORPHA:51608 | Generalized arterial calcification of infancy | | | | 151 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | ENPP1 CL E G H | 5167 | 3356 | OMIM:613312 | Hypophosphatemic rickets, autosomal recessive, 2 | | | | 151 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | FAH CL E G H | 2184 | 3579 | OMIM:276700 | Tyrosinemia, type I | | | | 107 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | FAM111A CL E G H | 63901 | 24725 | OMIM:127000 | Kenny-caffey syndrome, type 2 | | | | 8 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | FAM20C CL E G H | 56975 | 22140 | OMIM:259775 | Raine syndrome | . | | | 35 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | FGF23 CL E G H | 8074 | 3680 | ORPHA:89937 | Autosomal dominant hypophosphatemic rickets | HP:0040281 - Very frequent | | | 51 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | FGF23 CL E G H | 8074 | 3680 | OMIM:193100 | Hypophosphatemic rickets, autosomal dominant | . | | | 51 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | GABRA3 CL E G H | 2556 | 4077 | ORPHA:79102 | Thyrotoxic periodic paralysis | | | | | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | GATM CL E G H | 2628 | 4175 | OMIM:134600 | Fanconi renotubular syndrome 1 | . | | | 86 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | GATM CL E G H | 2628 | 4175 | ORPHA:3337 | Primary Fanconi renotubular syndrome | HP:0040282 - Frequent | | | 86 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | GCM2 CL E G H | 9247 | 4198 | ORPHA:99879 | Familial isolated hyperparathyroidism | HP:0040281 - Very frequent | | | 51 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | GNAS CL E G H | 2778 | 4392 | ORPHA:562 | McCune-Albright syndrome | HP:0040284 - Very rare | | | 101 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | HNF4A CL E G H | 3172 | 5024 | OMIM:616026 | Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young | | | | 138 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | HNF4A CL E G H | 3172 | 5024 | ORPHA:263455 | Hyperinsulinism due to HNF4A deficiency | | | | 138 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | HRAS CL E G H | 3265 | 5173 | ORPHA:2874 | Phakomatosis pigmentokeratotica | | | | 113 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | HRAS CL E G H | 3265 | 5173 | OMIM:163200 | Schimmelpenning-Feuerstein-Mims syndrome | | | | 113 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | INPPL1 CL E G H | 3636 | 6080 | OMIM:258480 | OPSISMODYSPLASIA | HP:0040283 - Occasional | | | 18 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | KCNJ18 CL E G H | 100134444 | 39080 | ORPHA:79102 | Thyrotoxic periodic paralysis | | | | 10 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | KRAS CL E G H | 3845 | 6407 | OMIM:163200 | Schimmelpenning-Feuerstein-Mims syndrome | | | | 196 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | MEN1 CL E G H | 4221 | 7010 | ORPHA:99879 | Familial isolated hyperparathyroidism | HP:0040281 - Very frequent | | | 462 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | NAB2 CL E G H | 4665 | 7627 | ORPHA:2126 | Solitary fibrous tumor/hemangiopericytoma | | | | | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | NDUFAF6 CL E G H | 137682 | 28625 | OMIM:618913 | FANCONI RENOTUBULAR SYNDROME 5; FRTS5 | | | | 39 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | NDUFAF6 CL E G H | 137682 | 28625 | ORPHA:3337 | Primary Fanconi renotubular syndrome | HP:0040282 - Frequent | | | 39 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | NHERF1 CL E G H | 9368 | 11075 | OMIM:612287 | Nephrolithiasis/osteoporosis, hypophosphatemic, 2 | . | | | | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | NRAS CL E G H | 4893 | 7989 | OMIM:163200 | Schimmelpenning-Feuerstein-Mims syndrome | | | | 102 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | OCRL CL E G H | 4952 | 8108 | OMIM:300555 | Dent disease 2 | | | | 88 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | OCRL CL E G H | 4952 | 8108 | ORPHA:534 | Oculocerebrorenal syndrome of Lowe | HP:0040283 - Occasional | | | 88 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | PHEX CL E G H | 5251 | 8918 | OMIM:307800 | Hypophosphatemic rickets, X-linked dominant | . | | | 217 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | PHEX CL E G H | 5251 | 8918 | ORPHA:89936 | X-linked hypophosphatemia | HP:0040281 - Very frequent | | | 217 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | POLRMT CL E G H | 5442 | 9200 | OMIM:619743 | COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 55; COXPD55 | | | | 1 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | PTH1R CL E G H | 5745 | 9608 | OMIM:156400 | Metaphyseal chondrodysplasia, Jansen type | . | | | 58 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | SLC2A2 CL E G H | 6514 | 11006 | OMIM:227810 | Fanconi-Bickel syndrome | . | | | 71 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | SLC2A2 CL E G H | 6514 | 11006 | ORPHA:2088 | Fanconi-Bickel syndrome | HP:0040281 - Very frequent | | | 71 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | SLC34A1 CL E G H | 6569 | 11019 | OMIM:613388 | Fanconi renotubular syndrome 2 | . | | | 47 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | SLC34A1 CL E G H | 6569 | 11019 | ORPHA:157215 | Hereditary hypophosphatemic rickets with hypercalciuria | HP:0040281 - Very frequent | | | 47 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | SLC34A1 CL E G H | 6569 | 11019 | OMIM:616963 | HYPERCALCEMIA, INFANTILE, 2; HCINF2 | | | | 47 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | SLC34A1 CL E G H | 6569 | 11019 | OMIM:612286 | Nephrolithiasis/osteoporosis, hypophosphatemic, 1 | . | | | 47 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | SLC34A1 CL E G H | 6569 | 11019 | ORPHA:3337 | Primary Fanconi renotubular syndrome | HP:0040282 - Frequent | | | 47 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | SLC34A3 CL E G H | 142680 | 20305 | ORPHA:157215 | Hereditary hypophosphatemic rickets with hypercalciuria | HP:0040281 - Very frequent | | | 52 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | SLC34A3 CL E G H | 142680 | 20305 | OMIM:241530 | Hypophosphatemic rickets with hypercalciuria, hereditary | . | | | 52 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | SNX10 CL E G H | 29887 | 14974 | ORPHA:667 | Autosomal recessive malignant osteopetrosis | HP:0040283 - Occasional | | | 2 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | STAT6 CL E G H | 6778 | 11368 | ORPHA:2126 | Solitary fibrous tumor/hemangiopericytoma | | | | 1 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | TCIRG1 CL E G H | 10312 | 11647 | ORPHA:667 | Autosomal recessive malignant osteopetrosis | HP:0040283 - Occasional | | | 82 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | TNFSF11 CL E G H | 8600 | 11926 | ORPHA:667 | Autosomal recessive malignant osteopetrosis | HP:0040283 - Occasional | | | 44 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | VDR CL E G H | 7421 | 12679 | ORPHA:93160 | Hypocalcemic vitamin D-resistant rickets | HP:0040281 - Very frequent | | | 104 | | |
HP:0002148 | HP:0002148 | Hypophosphatemia | 0 | VDR CL E G H | 7421 | 12679 | OMIM:277440 | Vitamin d-dependent rickets, type 2A | . | | | 104 | | |
HP:0002148 | HP:0004912 | Hypophosphatemic rickets | 1 | ABCC6 CL E G H | 368 | 57 | OMIM:614473 | Arterial calcification, generalized, of infancy, 2 | HP:0040283 - Occasional | | | 415 | | |
HP:0002148 | HP:0004912 | Hypophosphatemic rickets | 1 | ABCC6 CL E G H | 368 | 57 | ORPHA:51608 | Generalized arterial calcification of infancy | HP:0040282 - Frequent | | | 415 | | |
HP:0002148 | HP:0008285 | Transient hypophosphatemia | 1 | CACNA1S CL E G H | 779 | 1397 | ORPHA:79102 | Thyrotoxic periodic paralysis | HP:0040281 - Very frequent | | | 247 | | |
HP:0002148 | HP:0004912 | Hypophosphatemic rickets | 1 | CLCN5 CL E G H | 1184 | 2023 | OMIM:300554 | Hypophosphatemic rickets, X-linked recessive | . | | | 112 | | |
HP:0002148 | HP:0004912 | Hypophosphatemic rickets | 1 | CTNS CL E G H | 1497 | 2518 | OMIM:219800 | Cystinosis, nephropathic | . | | | 178 | | |
HP:0002148 | HP:0004912 | Hypophosphatemic rickets | 1 | DMP1 CL E G H | 1758 | 2932 | ORPHA:289176 | Autosomal recessive hypophosphatemic rickets | HP:0040280 - Obligate | | | 48 | | |
HP:0002148 | HP:0008732 | Renal hypophosphatemia | 1 | DMP1 CL E G H | 1758 | 2932 | ORPHA:289176 | Autosomal recessive hypophosphatemic rickets | HP:0040281 - Very frequent | | | 48 | | |
HP:0002148 | HP:0004912 | Hypophosphatemic rickets | 1 | DMP1 CL E G H | 1758 | 2932 | OMIM:241520 | Hypophosphatemic rickets, autosomal recessive | . | | | 48 | | |
HP:0002148 | HP:0004912 | Hypophosphatemic rickets | 1 | EHHADH CL E G H | 1962 | 3247 | ORPHA:3337 | Primary Fanconi renotubular syndrome | HP:0040282 - Frequent | | | 2 | | |
HP:0002148 | HP:0004912 | Hypophosphatemic rickets | 1 | ENPP1 CL E G H | 5167 | 3356 | OMIM:208000 | Arterial calcification, generalized, of infancy, 1 | HP:0040283 - Occasional | | | 151 | | |
HP:0002148 | HP:0004912 | Hypophosphatemic rickets | 1 | ENPP1 CL E G H | 5167 | 3356 | ORPHA:289176 | Autosomal recessive hypophosphatemic rickets | HP:0040280 - Obligate | | | 151 | | |
HP:0002148 | HP:0008732 | Renal hypophosphatemia | 1 | ENPP1 CL E G H | 5167 | 3356 | ORPHA:289176 | Autosomal recessive hypophosphatemic rickets | HP:0040281 - Very frequent | | | 151 | | |
HP:0002148 | HP:0004912 | Hypophosphatemic rickets | 1 | ENPP1 CL E G H | 5167 | 3356 | ORPHA:51608 | Generalized arterial calcification of infancy | HP:0040282 - Frequent | | | 151 | | |
HP:0002148 | HP:0004912 | Hypophosphatemic rickets | 1 | ENPP1 CL E G H | 5167 | 3356 | OMIM:613312 | Hypophosphatemic rickets, autosomal recessive, 2 | . | | | 151 | | |
HP:0002148 | HP:0004912 | Hypophosphatemic rickets | 1 | FAH CL E G H | 2184 | 3579 | OMIM:276700 | Tyrosinemia, type I | . | | | 107 | | |
HP:0002148 | HP:0008285 | Transient hypophosphatemia | 1 | FAM111A CL E G H | 63901 | 24725 | OMIM:127000 | Kenny-caffey syndrome, type 2 | . | | | 8 | | |
HP:0002148 | HP:0004912 | Hypophosphatemic rickets | 1 | FGF23 CL E G H | 8074 | 3680 | OMIM:193100 | Hypophosphatemic rickets, autosomal dominant | . | | | 51 | | |
HP:0002148 | HP:0008285 | Transient hypophosphatemia | 1 | GABRA3 CL E G H | 2556 | 4077 | ORPHA:79102 | Thyrotoxic periodic paralysis | HP:0040281 - Very frequent | | | | | |
HP:0002148 | HP:0004912 | Hypophosphatemic rickets | 1 | GATM CL E G H | 2628 | 4175 | ORPHA:3337 | Primary Fanconi renotubular syndrome | HP:0040282 - Frequent | | | 86 | | |
HP:0002148 | HP:0004912 | Hypophosphatemic rickets | 1 | HNF4A CL E G H | 3172 | 5024 | ORPHA:263455 | Hyperinsulinism due to HNF4A deficiency | HP:0040282 - Frequent | | | 138 | | |
HP:0002148 | HP:0004912 | Hypophosphatemic rickets | 1 | HRAS CL E G H | 3265 | 5173 | ORPHA:2874 | Phakomatosis pigmentokeratotica | | | | 113 | | |
HP:0002148 | HP:0004912 | Hypophosphatemic rickets | 1 | HRAS CL E G H | 3265 | 5173 | OMIM:163200 | Schimmelpenning-Feuerstein-Mims syndrome | . | | | 113 | | |
HP:0002148 | HP:0008285 | Transient hypophosphatemia | 1 | KCNJ18 CL E G H | 100134444 | 39080 | ORPHA:79102 | Thyrotoxic periodic paralysis | HP:0040281 - Very frequent | | | 10 | | |
HP:0002148 | HP:0004912 | Hypophosphatemic rickets | 1 | KRAS CL E G H | 3845 | 6407 | OMIM:163200 | Schimmelpenning-Feuerstein-Mims syndrome | . | | | 196 | | |
HP:0002148 | HP:0004912 | Hypophosphatemic rickets | 1 | NAB2 CL E G H | 4665 | 7627 | ORPHA:2126 | Solitary fibrous tumor/hemangiopericytoma | HP:0040284 - Very rare | | | | | |
HP:0002148 | HP:0004912 | Hypophosphatemic rickets | 1 | NDUFAF6 CL E G H | 137682 | 28625 | OMIM:618913 | FANCONI RENOTUBULAR SYNDROME 5; FRTS5 | | | | 39 | | |
HP:0002148 | HP:0004912 | Hypophosphatemic rickets | 1 | NDUFAF6 CL E G H | 137682 | 28625 | ORPHA:3337 | Primary Fanconi renotubular syndrome | HP:0040282 - Frequent | | | 39 | | |
HP:0002148 | HP:0004912 | Hypophosphatemic rickets | 1 | NRAS CL E G H | 4893 | 7989 | OMIM:163200 | Schimmelpenning-Feuerstein-Mims syndrome | . | | | 102 | | |
HP:0002148 | HP:0004912 | Hypophosphatemic rickets | 1 | PHEX CL E G H | 5251 | 8918 | OMIM:307800 | Hypophosphatemic rickets, X-linked dominant | . | | | 217 | | |
HP:0002148 | HP:0004912 | Hypophosphatemic rickets | 1 | POLRMT CL E G H | 5442 | 9200 | OMIM:619743 | COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 55; COXPD55 | | | | 1 | | |
HP:0002148 | HP:0004912 | Hypophosphatemic rickets | 1 | SLC34A1 CL E G H | 6569 | 11019 | ORPHA:157215 | Hereditary hypophosphatemic rickets with hypercalciuria | HP:0040281 - Very frequent | | | 47 | | |
HP:0002148 | HP:0004912 | Hypophosphatemic rickets | 1 | SLC34A1 CL E G H | 6569 | 11019 | ORPHA:3337 | Primary Fanconi renotubular syndrome | HP:0040282 - Frequent | | | 47 | | |
HP:0002148 | HP:0004912 | Hypophosphatemic rickets | 1 | SLC34A3 CL E G H | 142680 | 20305 | ORPHA:157215 | Hereditary hypophosphatemic rickets with hypercalciuria | HP:0040281 - Very frequent | | | 52 | | |
HP:0002148 | HP:0004912 | Hypophosphatemic rickets | 1 | SLC34A3 CL E G H | 142680 | 20305 | OMIM:241530 | Hypophosphatemic rickets with hypercalciuria, hereditary | . | | | 52 | | |
HP:0002148 | HP:0004912 | Hypophosphatemic rickets | 1 | STAT6 CL E G H | 6778 | 11368 | ORPHA:2126 | Solitary fibrous tumor/hemangiopericytoma | HP:0040284 - Very rare | | | 1 | | |