Mental retardation, severe to profound
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:
Christianson syndrome | (Orphanet:85278) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5 | (OMIM:613477) |
Infantile cerebellar-retinal degeneration | (Orphanet:313850) |
Lissencephaly due to TUBA1A mutation | (Orphanet:171680) |