Normal cognition
Symptom Information:
Symptom ID: | OMIM : No Id available | ||||
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Database Frequency: | 7 / 7739 | ||||
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All diseases associated with this symptom:
AMYOTROPHIC LATERAL SCLEROSIS 16, JUVENILE | (OMIM:614373) |
Autosomal recessive limb-girdle muscular dystrophy type 2N | (Orphanet:206559) |
Childhood encephalopathy due to thiamine pyrophosphokinase deficiency | (Orphanet:293955) |
Cholestasis - pigmentary retinopathy - cleft palate | (Orphanet:1415) |
LEBER OPTIC ATROPHY AND DYSTONIA | (OMIM:500001) |
Pierson syndrome | (Orphanet:2670) |
[DEL] SENGERS SYNDROME | (OMIM:212350) |