Microcephaly, mild
Symptom Information:
Symptom ID: | OMIM : No Id available | |||
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HPO:
MedDRA: |
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Database Frequency: | 4 / 7739 | |||
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All diseases associated with this symptom:
ARTHROGRYPOSIS, DISTAL, TYPE 2E | (OMIM:121070) |
Bilateral generalized polymicrogyria | (Orphanet:208447) |
Focal dermal hypoplasia | (Orphanet:2092) |
Hepatoencephalopathy due to combined oxidative phosphorylation deficiency type 1 | (Orphanet:137681) |