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Disease association ontology term - MONDO:0016106 - progressive muscular dystrophy

Term summary

ID
MONDO:0016106
Name
progressive muscular dystrophy
Ontology or CV name
Disease association

Parents

Annotation

Disease association

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

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

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

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MONDO:0011266 - myotonic dystrophy type 2

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MONDO:0958176 - oculopharyngeal muscular dystrophy 1

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MONDO:0014800 - progressive scapulohumeroperoneal distal myopathy

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MONDO:0010684 - X-linked myopathy with excessive autophagy

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