Mental retardation, severe to profound

Symptom Information:

Symptom ID: OMIM : No Id available
Synonyms:
Quality:
Cross references:
OMIM: "Mental retardation, severe to profound" [OMIM:Mental retardation, severe to profound]
Is a (Direct Parents):
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 4 / 7739
Resource:

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)