Reduced white matter volume
Symptom Information:
Symptom ID: | OMIM : No Id available | |
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Database Frequency: | 3 / 7739 | |
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All diseases associated with this symptom:
PORENCEPHALY 2 | (OMIM:614483) |
Porencephaly-microcephaly-bilateral congenital cataract syndrome | (Orphanet:306547) |
RETT SYNDROME, CONGENITAL VARIANT | (OMIM:613454) |