Microcephaly, severe
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:
MICROCEPHALY 3, PRIMARY, AUTOSOMAL RECESSIVE | (OMIM:604804) |
MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1 | (OMIM:257300) |
Microcephalic primordial dwarfism due to ZNF335 deficiency | (Orphanet:329228) |
Microcephalic primordial dwarfism, Dauber type | (Orphanet:319675) |