Arthrogryposis multiplex in severe cases
Symptom Information:
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Symptom ID:
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OMIM : No Id available
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Synonyms:
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Quality:
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Cross references:
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| OMIM: "Arthrogryposis multiplex in severe cases" [OMIM:Arthrogryposis multiplex in severe cases] |
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Is a (Direct Parents):
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Is a (Whole tree):
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HPO:
MedDRA:
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Database Frequency:
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4 / 7739
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Resource:
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All diseases associated with this symptom:
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MYASTHENIC SYNDROME, CONGENITAL, 1B, FAST-CHANNEL
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(OMIM:608930)
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MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL
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(OMIM:605809)
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MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINERECEPTOR DEFICIENCY
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(OMIM:608931)
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Presynaptic congenital myasthenic syndromes
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(Orphanet:98914)
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