Diabetes insipidus
Symptom Information:
| Symptom ID: | HPO:0000873 | |||||||||
| Synonyms: |
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HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the endocrine system(HPO:0000818) Diabetes insipidus(HPO:0000873) MedDRA: Endocrine disorders(MedDRA:10014698) Hypothalamus and pituitary gland disorders(MedDRA:10021112) Posterior pituitary disorders(MedDRA:10036361) Diabetes insipidus(HPO:0000873) |
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| Database Frequency: | 34 / 7739 | |||||||||
| Resource: |
All diseases associated with this symptom:
| 14q22q23 microdeletion syndrome | (Orphanet:264200) |
| Acquired central diabetes insipidus | (Orphanet:95626) |
| Alström syndrome | (Orphanet:64) |
| Arthrogryposis - renal dysfunction - cholestasis | (Orphanet:2697) |
| Bardet-Biedl syndrome 12 | (OMIM:615989) |
| CULLER-JONES SYNDROME | (OMIM:615849) |
| Carbamoylphosphate synthetase deficiency | (Orphanet:147) |
| Central diabetes insipidus | (Orphanet:178029) |
| Chronic hiccup | (Orphanet:396) |
| Congenital central diabetes insipidus | (Orphanet:95501) |
| Cystinosis | (Orphanet:213) |
| DIABETES INSIPIDUS, NEPHROGENIC, X-LINKED | (OMIM:304800) |
| Erdheim-Chester disease | (Orphanet:35687) |
| Fabry disease | (Orphanet:324) |
| Giant cell arteritis | (Orphanet:397) |
| Granulomatosis with polyangiitis | (Orphanet:900) |
| Growth hormone insensitivity syndrome | (Orphanet:181393) |
| HOLOPROSENCEPHALY 2 | (OMIM:157170) |
| Hand-Schüller-Christian disease | (Orphanet:99873) |
| Hartsfield-Bixler-Demyer syndrome | (Orphanet:2117) |
| Hereditary central diabetes insipidus | (Orphanet:30925) |
| Holoprosencephaly | (Orphanet:2162) |
| Oculocerebrorenal syndrome | (Orphanet:534) |
| POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY | (OMIM:611087) |
| Pituitary stalk interruption syndrome | (Orphanet:95496) |
| Riboflavin transporter deficiency | (Orphanet:97229) |
| Septo-optic dysplasia | (Orphanet:3157) |
| WEBB-DATTANI SYNDROME | (OMIM:615926) |
| Wolfram syndrome | (Orphanet:3463) |
| Wolfram syndrome 1 | (OMIM:222300) |
| Wolfram syndrome 2 | (OMIM:604928) |
| Wolfram syndrome, mitochondrial form | (OMIM:598500) |
| Wolfram-like syndrome | (ORPHA:411590) |
| Xanthoma disseminatum | (Orphanet:158003) |