Abnormal renal morphology
Symptom Information:
Symptom ID: | HPO:0012210 | |||||||||||||
Synonyms: |
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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 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 morphology(HPO:0012210) MedDRA: Renal and urinary disorders(MedDRA:10038359) Nephropathy(HPO:0000112) Renal structural abnormalities and trauma(MedDRA:10038529) Abnormal renal morphology(HPO:0012210) |
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Database Frequency: | 18 / 7739 | |||||||||||||
Resource: |
All diseases associated with this symptom:
17p11.2 microduplication syndrome | (Orphanet:1713) |
ACRORENAL SYNDROME | (OMIM:102520) |
Acrorenal syndrome | (Orphanet:971) |
Alström syndrome | (Orphanet:64) |
Antley-Bixler syndrome | (Orphanet:83) |
Bardet-Biedl syndrome | (Orphanet:110) |
Bardet-Biedl syndrome 10 | (OMIM:615987) |
Bardet-Biedl syndrome 12 | (OMIM:615989) |
Bardet-Biedl syndrome 6 | (OMIM:605231) |
CORNELIA DE LANGE SYNDROME 1 | (OMIM:122470) |
Distal monosomy 3p | (Orphanet:1620) |
FANCONI ANEMIA, COMPLEMENTATION GROUP A | (OMIM:227650) |
FANCONI ANEMIA, COMPLEMENTATION GROUP C | (OMIM:227645) |
FANCONI ANEMIA, COMPLEMENTATION GROUP D2 | (OMIM:227646) |
FANCONI ANEMIA, COMPLEMENTATION GROUP I | (OMIM:609053) |
Renal cysts and diabetes syndrome | (Orphanet:93111) |
Smith-Magenis syndrome | (Orphanet:819) |
Wolfram syndrome 1 | (OMIM:222300) |