Global glomerulosclerosis
Symptom Information:
Symptom ID: | HPO:0004737 | ||
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 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) Abnormality of the nephron(HPO:0012575) Abnormality of the glomerulus(HPO:0000095) Glomerulosclerosis(HPO:0000096) Global glomerulosclerosis(HPO:0004737) MedDRA: |
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Database Frequency: | 3 / 7739 | ||
Resource: |
All diseases associated with this symptom:
BARTTER SYNDROME, TYPE 4A | (OMIM:602522) |
Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation | (Orphanet:324525) |
Infantile Bartter syndrome with deafness | (Orphanet:89938) |