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Disease association ontology term - MONDO:0003939 - muscle tissue disorder

Term summary

ID
MONDO:0003939
Name
muscle tissue disorder
Ontology or CV name
Disease association
Definition
A disease involving the muscle tissue.

Parents

Annotation

Disease association

MONDO:8000015 - 46,XY sex reversal 11

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MONDO:0100084 - alpha-actinopathy

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MONDO:0030847 - arthrogryposis, distal, type 1C

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MONDO:0032751 - arthrogryposis, distal, type 2B3

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MONDO:0014248 - autism spectrum disorder - epilepsy - arthrogryposis syndrome

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MONDO:0021018 - autosomal dominant limb-girdle muscular dystrophy type 1D (DNAJB6)

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MONDO:0012034 - autosomal dominant limb-girdle muscular dystrophy type 1F

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MONDO:0014532 - autosomal dominant mitochondrial myopathy with exercise intolerance

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MONDO:0012248 - autosomal recessive limb-girdle muscular dystrophy type 2K

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MONDO:0013162 - autosomal recessive limb-girdle muscular dystrophy type 2N

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MONDO:0014142 - autosomal recessive limb-girdle muscular dystrophy type 2T

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MONDO:0010977 - Brody myopathy

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MONDO:0011451 - cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1

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MONDO:0014051 - cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2

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MONDO:0014667 - cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 3

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MONDO:0014668 - cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 4

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MONDO:0015280 - cardiofaciocutaneous syndrome

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MONDO:0007265 - cardiofaciocutaneous syndrome 1

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MONDO:0014112 - cardiofaciocutaneous syndrome 2

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MONDO:0014113 - cardiofaciocutaneous syndrome 3

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MONDO:0014114 - cardiofaciocutaneous syndrome 4

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MONDO:0032592 - cardiomyopathy, dilated, 2c

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MONDO:0030300 - cardiomyopathy, dilated, 2D

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MONDO:0859358 - cardiomyopathy, dilated, 2H

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MONDO:0957545 - cardiomyopathy, dilated, 2I

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MONDO:0030330 - cardiomyopathy, familial restrictive, 6

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MONDO:0012557 - cardiomyopathy-hypotonia-lactic acidosis syndrome

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MONDO:0018947 - centronuclear myopathy

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MONDO:0013116 - congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome

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MONDO:0014023 - congenital muscular dystrophy with intellectual disability and severe epilepsy

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MONDO:0014896 - congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome

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MONDO:0859264 - congenital myopathy 11

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MONDO:0957224 - congenital myopathy 21 with early respiratory failure

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MONDO:0979229 - congenital myopathy 26

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MONDO:0980756 - congenital myopathy 28 with rigid spine

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MONDO:0008070 - congenital myopathy 2a, typical, autosomal dominant

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MONDO:0859517 - congenital myopathy 2b, severe infantile, autosomal recessive

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MONDO:0859523 - congenital myopathy 2c, severe infantile, autosomal dominant

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MONDO:0800341 - congenital myopathy 4A, autosomal dominant

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MONDO:0012239 - congenital myopathy 4B, autosomal recessive

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MONDO:0008409 - congenital myopathy 7A, myosin storage, autosomal dominant

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MONDO:0034109 - congenital myopathy with reduced type 2 muscle fibers

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MONDO:0008338 - contractures, pterygia, and spondylocarpotarsal fusion syndrome 1A

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MONDO:0009026 - Costello syndrome

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MONDO:0859571 - diaphragmatic hernia 4, with cardiovascular defects

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MONDO:0005021 - dilated cardiomyopathy

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MONDO:0012808 - dilated cardiomyopathy 1AA

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MONDO:0013198 - dilated cardiomyopathy 1EE

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MONDO:0013339 - dilated cardiomyopathy 1GG

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MONDO:0014073 - dilated cardiomyopathy 1II

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MONDO:0013261 - dilated cardiomyopathy 1R

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MONDO:0013262 - dilated cardiomyopathy 1S

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MONDO:0012556 - DK1-congenital disorder of glycosylation

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MONDO:0013049 - DPM3-congenital disorder of glycosylation

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MONDO:0015487 - fatal infantile encephalocardiomyopathy

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MONDO:0013472 - fatal infantile hypertonic myofibrillar myopathy

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MONDO:0010912 - fibrosis of extraocular muscles, congenital, 3A, with or without extraocular involvement

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MONDO:0008675 - Freeman-Sheldon syndrome

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MONDO:0017694 - glycogen storage disease due to acid maltase deficiency, infantile onset

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MONDO:0018485 - glycogen storage disease due to acid maltase deficiency, late-onset

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MONDO:0009290 - glycogen storage disease II

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MONDO:0009706 - hereditary myopathy with lactic acidosis due to ISCU deficiency

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MONDO:0010606 - hernia, anterior diaphragmatic

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MONDO:0005045 - hypertrophic cardiomyopathy

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MONDO:0008647 - hypertrophic cardiomyopathy 1

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MONDO:0012112 - hypertrophic cardiomyopathy 10

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MONDO:0012799 - hypertrophic cardiomyopathy 11

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MONDO:0013197 - hypertrophic cardiomyopathy 14

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MONDO:0010946 - hypertrophic cardiomyopathy 6

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MONDO:0012111 - hypertrophic cardiomyopathy 8

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MONDO:0009637 - inborn mitochondrial myopathy

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MONDO:0000507 - inclusion body myopathy with Paget disease of bone and frontotemporal dementia

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MONDO:0008178 - inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1

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MONDO:0009867 - lethal congenital glycogen storage disease of heart

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MONDO:0011246 - megaconial type congenital muscular dystrophy

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MONDO:0030935 - mitochondrial complex 2 deficiency, nuclear type 2

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MONDO:0030937 - mitochondrial complex 2 deficiency, nuclear type 3

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MONDO:0030974 - mitochondrial complex 2 deficiency, nuclear type 4

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MONDO:0100294 - mitochondrial complex II deficiency, nuclear type 1

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MONDO:0014062 - mitochondrial DNA deletion syndrome with progressive myopathy

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MONDO:0013350 - mitochondrial DNA depletion syndrome 4b

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MONDO:0012792 - mitochondrial DNA depletion syndrome 8a

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MONDO:0020714 - mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy

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MONDO:0044714 - mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome

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MONDO:0009282 - multiple acyl-CoA dehydrogenase deficiency

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MONDO:0020121 - muscular dystrophy

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MONDO:0009682 - muscular dystrophy, congenital, with rapid progression

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MONDO:0957270 - muscular dystrophy, limb-girdle, autosomal recessive 28

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MONDO:0009364 - muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A1

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MONDO:0014140 - muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A14

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MONDO:0013154 - muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A2

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MONDO:0033556 - muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 15

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MONDO:0013159 - muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B1

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MONDO:0014141 - muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B14

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MONDO:0013160 - muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B2

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MONDO:0000171 - muscular dystrophy-dystroglycanopathy, type A

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MONDO:0008050 - MYH7-related skeletal myopathy

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MONDO:0030927 - myofibrillar myopathy 11

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MONDO:0012130 - myofibrillar myopathy 2

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MONDO:0014220 - myopathy due to myoadenylate deaminase deficiency

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MONDO:0009703 - myopathy with abnormal lipid metabolism

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MONDO:0009709 - myopathy, centronuclear, 2

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MONDO:0032852 - myopathy, congenital, with structured cores and z-line abnormalities

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MONDO:0014877 - myopathy, distal, 5

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MONDO:0032853 - myopathy, distal, 6, adult-onset, autosomal dominant

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MONDO:0024553 - myopathy, lactic acidosis, and sideroblastic anemia 1

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MONDO:0013307 - myopathy, lactic acidosis, and sideroblastic anemia 2

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MONDO:0859168 - myopathy, myofibrillar, 12, infantile-onset, with cardiomyopathy

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MONDO:0976133 - myopathy, myofibrillar, 13, with rimmed vacuoles

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MONDO:0009708 - myopathy, myosin storage, autosomal recessive

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MONDO:0011577 - myopathy, proximal, and ophthalmoplegia

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MONDO:0011266 - myotonic dystrophy type 2

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MONDO:0018958 - nemaline myopathy

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MONDO:0009725 - nemaline myopathy 2

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MONDO:0012538 - nemaline myopathy 7

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MONDO:0018997 - Noonan syndrome

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MONDO:0033669 - Noonan syndrome 13

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MONDO:0012371 - Noonan syndrome 3

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MONDO:0013186 - Noonan syndrome 6

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MONDO:0054588 - Noonan syndrome-like disorder with loose anagen hair 2

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MONDO:0958176 - oculopharyngeal muscular dystrophy 1

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MONDO:0013968 - PGM1-congenital disorder of glycosylation

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MONDO:0014526 - polyglucosan body myopathy type 2

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MONDO:0005181 - progressive external ophthalmoplegia

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MONDO:0024528 - progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1

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MONDO:0012238 - progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2

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MONDO:0013117 - progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5

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MONDO:0009783 - progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 1

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MONDO:0014656 - progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2

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MONDO:0020845 - progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5

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MONDO:0957993 - progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal recessive 6

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MONDO:0014800 - progressive scapulohumeroperoneal distal myopathy

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MONDO:0011835 - sensory ataxic neuropathy, dysarthria, and ophthalmoparesis

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MONDO:0014784 - severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome

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MONDO:0859173 - sick sinus syndrome 4

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MONDO:0008016 - trismus-pseudocamptodactyly syndrome

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MONDO:0008685 - Wolff-Parkinson-White syndrome

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MONDO:0010684 - X-linked myopathy with excessive autophagy

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MONDO:0010683 - X-linked myotubular myopathy

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MONDO:0100138 - X-linked recessive mitochondrial myopathy

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