Facial weakness, mild
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:
Autosomal recessive limb-girdle muscular dystrophy due to desmin deficiency | (Orphanet:363543) |
Autosomal recessive limb-girdle muscular dystrophy type 2L | (Orphanet:206549) |
COLD-INDUCED SWEATING SYNDROME 2 | (OMIM:610313) |
Congenital muscular dystrophy, Ullrich type | (Orphanet:75840) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 6 | (OMIM:608840) |
Steinert myotonic dystrophy | (Orphanet:273) |