'Stiffness'
Symptom Information:
Symptom ID: | OMIM : No Id available | |||
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Is a (Whole tree): |
HPO:
MedDRA: |
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Database Frequency: | 5 / 7739 | |||
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All diseases associated with this symptom:
6-pyruvoyl-tetrahydropterin synthase deficiency | (Orphanet:13) |
Congenital myopathy with excess of thin filaments | (Orphanet:98904) |
Fatal infantile hypertonic myofibrillar myopathy | (Orphanet:280553) |
Hepatoencephalopathy due to combined oxidative phosphorylation deficiency type 1 | (Orphanet:137681) |
Pantothenate kinase-associated neurodegeneration | (Orphanet:157850) |