Difficulty climbing stairs

Symptom Information:

Symptom ID: HPO:0003551
Synonyms:
Difficulty walking up stairs [HPO:0003551]
Difficulty climbing stairs [OMIM:Difficulty climbing stairs]
Difficulty walking up stairs [OMIM:Difficulty walking up stairs]
Quality:
Cross references:
OMIM: "Difficulty climbing stairs" [OMIM:Difficulty climbing stairs]
OMIM: "Difficulty walking up stairs" [OMIM:Difficulty walking up stairs]
Is a (Direct Parents):
HPO         Functional motor problems
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:
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)