Small cerebellum
Symptom Information:
Symptom ID: | OMIM : No Id available | ||
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Database Frequency: | 6 / 7739 | ||
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All diseases associated with this symptom:
MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4 | (OMIM:615228) |
Microlissencephaly | (Orphanet:1083) |
Microphthalmia with brain and digit anomalies | (Orphanet:139471) |
Pontocerebellar hypoplasia type 3 | (Orphanet:97249) |
SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION,LETHAL | (OMIM:602613) |
SLC35A2-CDG | (Orphanet:356961) |