Abnormal renal physiology
Symptom Information:
Symptom ID: | HPO:0012211 | ||||||||||||
Synonyms: |
|
||||||||||||
Quality: | |||||||||||||
Cross references: |
|
||||||||||||
Is a (Direct Parents): |
|
||||||||||||
Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the genitourinary system(HPO:0000119) Abnormality of the urinary system(HPO:0000079) Abnormality of the upper urinary tract(HPO:0010935) Abnormality of the kidney(HPO:0000077) Abnormal renal physiology(HPO:0012211) Abnormality of the urinary system physiology(HPO:0011277) Abnormal renal physiology(HPO:0012211) MedDRA: |
||||||||||||
Database Frequency: | 23 / 7739 | ||||||||||||
Resource: |
All diseases associated with this symptom:
1p36 deletion syndrome | (Orphanet:1606) |
AA amyloidosis | (Orphanet:85445) |
Aceruloplasminemia | (Orphanet:48818) |
Alström syndrome | (Orphanet:64) |
Bardet-Biedl syndrome 10 | (OMIM:615987) |
Bardet-Biedl syndrome 17 | (OMIM:615994) |
Bardet-Biedl syndrome 6 | (OMIM:605231) |
Bardet-Biedl syndrome 9 | (OMIM:615986) |
Bartter syndrome with hypocalcemia | (Orphanet:263417) |
CORNELIA DE LANGE SYNDROME 1 | (OMIM:122470) |
Congenital thrombotic thrombocytopenic purpura due to ADAMTS-13 deficiency | (Orphanet:93583) |
Cushing syndrome | (Orphanet:553) |
Cystinuria | (Orphanet:214) |
Encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome | (Orphanet:319678) |
Fabry disease | (Orphanet:324) |
Familial dysautonomia | (Orphanet:1764) |
Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation | (Orphanet:324525) |
Joubert syndrome 2 | (OMIM:608091) |
Leigh syndrome | (Orphanet:506) |
MEDULLARY CYSTIC KIDNEY DISEASE 1 | (OMIM:174000) |
RENAL DYSPLASIA, CYSTIC, SUSCEPTIBILITY TO | (OMIM:601331) |
Refsum disease | (Orphanet:773) |
Thrombotic thrombocytopenic purpura | (Orphanet:54057) |