Muscular dystrophy
Symptom Information:
Symptom ID: | HPO:0003560 | ||||||||||||||
Synonyms: |
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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 morphology(HPO:0011805) Muscular dystrophy(HPO:0003560) MedDRA: Musculoskeletal and connective tissue disorders(MedDRA:10028395) Musculoskeletal and connective tissue disorders congenital(MedDRA:10028396) Non-site specific muscle disorders congenital(MedDRA:10029512) Muscular dystrophy(HPO:0003560) |
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Database Frequency: | 88 / 7739 | ||||||||||||||
Resource: |
All diseases associated with this symptom:
ADRENAL HYPOPLASIA, CONGENITAL | (OMIM:300200) |
AMINO ACIDURIA WITH MENTAL DEFICIENCY, DWARFISM, MUSCULAR DYSTROPHY,OSTEOPOROSIS, AND ACIDOSIS | (OMIM:204730) |
AMYOTROPHIC LATERAL SCLEROSIS 20 | (OMIM:615426) |
Alpha-crystallinopathy | (Orphanet:98910) |
Antenatal multiminicore disease with arthrogryposis multiplex congenita | (Orphanet:178148) |
Autosomal dominant Emery-Dreifuss muscular dystrophy | (Orphanet:98853) |
Autosomal dominant limb-girdle muscular dystrophy type 1A | (Orphanet:266) |
Autosomal dominant limb-girdle muscular dystrophy type 1B | (Orphanet:264) |
Autosomal dominant limb-girdle muscular dystrophy type 1C | (Orphanet:265) |
Autosomal dominant limb-girdle muscular dystrophy type 1D | (Orphanet:34516) |
Autosomal dominant limb-girdle muscular dystrophy type 1F | (Orphanet:55595) |
Autosomal dominant limb-girdle muscular dystrophy type 1H | (Orphanet:238755) |
Autosomal recessive Emery-Dreifuss muscular dystrophy | (Orphanet:98855) |
Autosomal recessive limb girdle muscular dystrophy type 2A | (Orphanet:267) |
Autosomal recessive limb-girdle muscular dystrophy due to desmin deficiency | (Orphanet:363543) |
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 2H | (Orphanet:1878) |
Autosomal recessive limb-girdle muscular dystrophy type 2I | (Orphanet:34515) |
Autosomal recessive limb-girdle muscular dystrophy type 2J | (Orphanet:140922) |
Autosomal recessive limb-girdle muscular dystrophy type 2K | (Orphanet:86812) |
Autosomal recessive limb-girdle muscular dystrophy type 2L | (Orphanet:206549) |
Autosomal recessive limb-girdle muscular dystrophy type 2M | (Orphanet:206554) |
Autosomal recessive limb-girdle muscular dystrophy type 2N | (Orphanet:206559) |
Autosomal recessive limb-girdle muscular dystrophy type 2O | (Orphanet:206564) |
Autosomal recessive limb-girdle muscular dystrophy type 2P | (Orphanet:280333) |
Autosomal recessive limb-girdle muscular dystrophy type 2Q | (Orphanet:254361) |
Autosomal recessive limb-girdle muscular dystrophy type 2T | (Orphanet:363623) |
Becker muscular dystrophy | (Orphanet:98895) |
Carney complex | (Orphanet:1359) |
Classic multiminicore myopathy | (Orphanet:324604) |
Congenital multicore myopathy with external ophthalmoplegia | (Orphanet:98905) |
Congenital muscular dystrophy due to phosphatidylcholine biosynthesis defect | (Orphanet:280671) |
Congenital muscular dystrophy type 1A | (Orphanet:258) |
DPM1-CDG | (Orphanet:79322) |
DPM3-CDG | (Orphanet:263494) |
Duchenne muscular dystrophy | (Orphanet:98896) |
EMERY-DREIFUSS MUSCULAR DYSTROPHY 4, AUTOSOMAL DOMINANT | (OMIM:612998) |
EMERY-DREIFUSS MUSCULAR DYSTROPHY 5, AUTOSOMAL DOMINANT | (OMIM:612999) |
EMERY-DREIFUSS MUSCULAR DYSTROPHY 7, AUTOSOMAL DOMINANT | (OMIM:614302) |
Emery-Dreifuss muscular dystrophy | (Orphanet:261) |
Epidermolysis bullosa simplex with muscular dystrophy | (Orphanet:257) |
Fatal infantile hypertonic myofibrillar myopathy | (Orphanet:280553) |
Generalized congenital lipodystrophy with myopathy | (Orphanet:228429) |
INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUTFRONTOTEMPORAL DEMENTIA 2 | (OMIM:615422) |
Isolated glycerol kinase deficiency | (Orphanet:408) |
Kearns-Sayre syndrome | (Orphanet:480) |
LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 6 | (OMIM:615980) |
Leprechaunism | (Orphanet:508) |
MELAS | (Orphanet:550) |
MIYOSHI MUSCULAR DYSTROPHY 1 | (OMIM:254130) |
MIYOSHI MUSCULAR DYSTROPHY 3 | (OMIM:613319) |
MUSCULAR DYSTROPHY, ADULT-ONSET, WITH LEUKOENCEPHALOPATHY | (OMIM:253590) |
MUSCULAR DYSTROPHY, BARNES TYPE | (OMIM:158800) |
MUSCULAR DYSTROPHY, CARDIAC TYPE | (OMIM:309930) |
MUSCULAR DYSTROPHY, CONGENITAL, MEROSIN-POSITIVE | (OMIM:609456) |
MUSCULAR DYSTROPHY, PROGRESSIVE PECTORODORSAL | (OMIM:310095) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 1 | (OMIM:236670) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 10 | (OMIM:615041) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 11 | (OMIM:615181) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 12 | (OMIM:615249) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 13 | (OMIM:615287) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 14 | (OMIM:615350) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 2 | (OMIM:613150) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 3 | (OMIM:253280) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 4 | (OMIM:253800) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 5 | (OMIM:613153) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 6 | (OMIM:613154) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 7 | (OMIM:614643) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 8 | (OMIM:614830) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 1 | (OMIM:613155) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 14 | (OMIM:615351) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 2 | (OMIM:613156) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 3 | (OMIM:613151) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 6 | (OMIM:608840) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUTMENTAL RETARDATION), TYPE B, 5 | (OMIM:606612) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION),TYPE B, 4 | (OMIM:613152) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 12 | (OMIM:616094) |
MYOPATHY, DISTAL, 3 | (OMIM:610099) |
Mitochondrial myopathy and sideroblastic anemia | (Orphanet:2598) |
Miyoshi myopathy | (Orphanet:45448) |
Muscular dystrophy, Selcen type | (Orphanet:199340) |
Steinert myotonic dystrophy | (Orphanet:273) |
Tibial muscular dystrophy | (Orphanet:609) |
VACUOLAR NEUROMYOPATHY | (OMIM:601846) |
Werner syndrome | (Orphanet:902) |
X-linked Emery-Dreifuss muscular dystrophy | (Orphanet:98863) |
[DEL] MUSCULAR DYSTROPHY, BECKER TYPE | (OMIM:300376) |