Hematuria, gross and microscopic
Symptom Information:
Symptom ID: | OMIM : No Id available | |
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Database Frequency: | 4 / 7739 | |
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All diseases associated with this symptom:
Autosomal dominant Alport syndrome | (Orphanet:88918) |
Autosomal recessive Alport syndrome | (Orphanet:88919) |
LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME | (OMIM:308940) |
X-linked Alport syndrome | (Orphanet:88917) |