Hypo- or areflexia
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:
Autosomal dominant Charcot-Marie-Tooth disease type 2N | (Orphanet:228174) |
Hereditary motor and sensory neuropathy, Okinawa type | (Orphanet:90117) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 4 | (OMIM:253800) |
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 3 | (OMIM:609286) |