Difficulty climbing stairs
Symptom Information:
Symptom ID: | HPO:0003551 | |||
Synonyms: |
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Quality: | ||||
Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the musculature(HPO:0003011) Abnormality of muscle physiology(HPO:0011804) Functional motor problems(HPO:0004302) Difficulty climbing stairs(HPO:0003551) MedDRA: |
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Database Frequency: | 23 / 7739 | |||
Resource: |
All diseases associated with this symptom:
Autosomal dominant limb-girdle muscular dystrophy type 1B | (Orphanet:264) |
Autosomal dominant limb-girdle muscular dystrophy type 1D | (Orphanet:34516) |
Autosomal recessive limb-girdle muscular dystrophy type 2B | (Orphanet:268) |
Autosomal recessive limb-girdle muscular dystrophy type 2G | (Orphanet:34514) |
Autosomal recessive limb-girdle muscular dystrophy type 2I | (Orphanet:34515) |
Autosomal recessive limb-girdle muscular dystrophy type 2K | (Orphanet:86812) |
Autosomal recessive limb-girdle muscular dystrophy type 2O | (Orphanet:206564) |
Autosomal recessive limb-girdle muscular dystrophy type 2Q | (Orphanet:254361) |
Autosomal recessive lower motor neuron disease with childhood onset | (Orphanet:206580) |
Congenital muscular dystrophy with cerebellar involvement | (Orphanet:370959) |
Duchenne muscular dystrophy | (Orphanet:98896) |
Early-onset myopathy with fatal cardiomyopathy | (Orphanet:289377) |
INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUTFRONTOTEMPORAL DEMENTIA 1 | (OMIM:167320) |
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia | (Orphanet:52430) |
MIYOSHI MUSCULAR DYSTROPHY 1 | (OMIM:254130) |
MIYOSHI MUSCULAR DYSTROPHY 3 | (OMIM:613319) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5 | (OMIM:606612) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 12 | (OMIM:616094) |
Miyoshi myopathy | (Orphanet:45448) |
Multiple acyl-CoA dehydrogenase deficiency | (Orphanet:26791) |
Muscle filaminopathy | (Orphanet:171445) |
NEMALINE MYOPATHY 6 | (OMIM:609273) |
X-linked myopathy with excessive autophagy | (Orphanet:25980) |