Poor motor development
Symptom Information:
Symptom ID: | OMIM : No Id available | |
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Database Frequency: | 3 / 7739 | |
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All diseases associated with this symptom:
HYDROCEPHALUS, NONSYNDROMIC, AUTOSOMAL RECESSIVE 1 | (OMIM:236600) |
MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICALMALFORMATIONS | (OMIM:604317) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 4 | (OMIM:253800) |