Muscular dystrophy

Symptom Information:

Symptom ID: HPO:0003560
Synonyms:
MUSCLE BIOPSY SHOWS DYSTROPHIC CHANGES [HPO:0003560]
Muscle dystrophy [Orphanet:44250]
Muscular Dystrophy [Orphanet:44250]
Muscle biopsy shows dystrophic changes [OMIM:Muscle biopsy shows dystrophic changes]
Muscular dystrophy [OMIM:Muscular dystrophy]
Muscle hypotrophy/atrophy/dystrophy/agenesis/amyotrophy [Orphanet:44250]
Muscular dystrophy [Orphanet:44250]
Muscular dystrophy [MedDRA:10028356]
Congenital hereditary muscular dystrophy [MedDRA:10028356]
Hereditary progressive muscular dystrophy [MedDRA:10028356]
Muscular dystrophies and other myopathies [MedDRA:10028356]
Muscular dystrophies and other myopathies, unspecified [MedDRA:10028356]
Muscular dystrophy NOS [MedDRA:10028356]
Other muscular dystrophies and myopathies [MedDRA:10028356]
Quality:
Cross references:
Orphanet:44250 "Muscle hypotrophy/atrophy/dystrophy/agenesis/amyotrophy" [Orphanet:44250]
OMIM: "Muscle biopsy shows dystrophic changes" [OMIM:Muscle biopsy shows dystrophic changes]
OMIM: "Muscular dystrophy" [OMIM:Muscular dystrophy]
UMLS:C0026850 "Muscular Dystrophy" [Orphanet:44250]
Is a (Direct Parents):
HPO         Abnormality of muscle morphology
Orphanet Muscle anomalies
MedDRA Non-site specific muscle disorders congenital
Orphanet Skeletal muscle atrophy
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)
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)