Polydipsia
Symptom Information:
| Symptom ID: | HPO:0001959 | ||||
| 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 nervous system(HPO:0000707) Abnormality of nervous system physiology(HPO:0012638) Abnormality of higher mental function(HPO:0011446) Behavioral abnormality(HPO:0000708) Polydipsia(HPO:0001959) MedDRA: Endocrine disorders(MedDRA:10014698) Hypothalamus and pituitary gland disorders(MedDRA:10021112) Posterior pituitary disorders(MedDRA:10036361) Polydipsia(HPO:0001959) |
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| Database Frequency: | 43 / 7739 | ||||
| Resource: |
All diseases associated with this symptom:
| Alström syndrome | (Orphanet:64) |
| Autosomal recessive medullary cystic kidney disease | (Orphanet:655) |
| BARTTER SYNDROME, ANTENATAL, TYPE 2 | (OMIM:241200) |
| Bardet-Biedl syndrome 10 | (OMIM:615987) |
| Bardet-Biedl syndrome 17 | (OMIM:615994) |
| Bartter syndrome | (Orphanet:112) |
| CYSTINOSIS, NEPHROPATHIC | (OMIM:219800) |
| Cystinosis | (Orphanet:213) |
| DIABETES INSIPIDUS, NEPHROGENIC, AUTOSOMAL | (OMIM:125800) |
| DIABETES INSIPIDUS, NEPHROGENIC, X-LINKED | (OMIM:304800) |
| DIABETES INSIPIDUS, NEUROHYPOPHYSEAL TYPE | (OMIM:304900) |
| DIABETES MELLITUS, INSULIN-DEPENDENT | (OMIM:222100) |
| Dent disease type 1 | (Orphanet:93622) |
| EAST syndrome | (Orphanet:199343) |
| Fabry disease | (Orphanet:324) |
| Familial hyperaldosteronism type 3 | (Orphanet:251274) |
| Familial hypomagnesemia - hypercalciuria - nephrocalcinosis | (Orphanet:31043) |
| Fanconi renotubular syndrome 1 | (OMIM:134600) |
| Gitelman syndrome | (Orphanet:358) |
| Insulin-resistance syndrome type A | (Orphanet:2297) |
| Joubert syndrome 5 | (OMIM:610188) |
| Leprechaunism | (Orphanet:508) |
| Maturity-onset diabetes of the young, type 4 | (OMIM:606392) |
| Maturity-onset diabetes of the young, type 9 | (OMIM:612225) |
| Neonatal severe primary hyperparathyroidism | (Orphanet:417) |
| Nephrogenic diabetes insipidus | (Orphanet:223) |
| Nephronophthisis 1 | (OMIM:256100) |
| Nephronophthisis 2 | (OMIM:602088) |
| Nephronophthisis 3 | (OMIM:604387) |
| Nephronophthisis 4 | (OMIM:606966) |
| Nephronophthisis 9 | (OMIM:613824) |
| Rabson-Mendenhall syndrome | (Orphanet:769) |
| Renal cysts and diabetes syndrome | (Orphanet:93111) |
| Renal glucosuria | (Orphanet:69076) |
| Senior-Boichis syndrome | (Orphanet:84081) |
| Senior-Loken syndrome | (Orphanet:3156) |
| Senior-Loken syndrome 1 | (OMIM:266900) |
| Senior-Loken syndrome 3 | (OMIM:606995) |
| Senior-Loken syndrome 4 | (OMIM:606996) |
| Senior-Loken syndrome 5 | (OMIM:609254) |
| Senior-Loken syndrome 6 | (OMIM:610189) |
| TERATOMA, PINEAL | (OMIM:273120) |
| Wilson disease | (Orphanet:905) |