DOID:0111188
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myofibrillar myopathy 9
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Aliases:
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Edstrom myopathy
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HIBM-ERF
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HMERF
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Hereditary inclusion body myopathy with early respiratory failure
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MFM-titinopathy
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MFM9
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MPRM
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Myofibrillar myopathy-titinopathy
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autosomal dominant distal myopathy with early respiratory failure
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hereditary myopathy with early respiratory failure
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myofibrillar myopathy 9 with early respiratory failure
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proximal myopathy with early respiratory muscle involvement
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Homo sapiens (human)
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DOID:0111188
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myofibrillar myopathy 9
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Aliases:
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Edstrom myopathy
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HIBM-ERF
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HMERF
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Hereditary inclusion body myopathy with early respiratory failure
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MFM-titinopathy
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MFM9
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MPRM
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Myofibrillar myopathy-titinopathy
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autosomal dominant distal myopathy with early respiratory failure
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hereditary myopathy with early respiratory failure
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myofibrillar myopathy 9 with early respiratory failure
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proximal myopathy with early respiratory muscle involvement
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Mus musculus (house mouse)
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DOID:0111189
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distal myopathy 3
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Aliases:
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MPD3
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distal muscular dystrophy 3
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distal myopathy type 3
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Mus musculus (house mouse)
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DOID:0111189
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distal myopathy 3
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Aliases:
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MPD3
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distal muscular dystrophy 3
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distal myopathy type 3
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Homo sapiens (human)
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DOID:0111190
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distal myopathy 4
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Aliases:
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MPD4
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distal ABD-filaminopathy
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distal muscular dystrophy 4
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distal myopathy with posterior leg and anterior hand involvement
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Homo sapiens (human)
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DOID:0111190
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distal myopathy 4
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Aliases:
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MPD4
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distal ABD-filaminopathy
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distal muscular dystrophy 4
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distal myopathy with posterior leg and anterior hand involvement
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Mus musculus (house mouse)
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DOID:0111193
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facioscapulohumeral muscular dystrophy 2
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Aliases:
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FSHD2
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facioscapulohumeral muscular dystrophy 1B
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facioscapulohumeral muscular dystrophy type 2
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Mus musculus (house mouse)
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DOID:0111193
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facioscapulohumeral muscular dystrophy 2
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Aliases:
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FSHD2
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facioscapulohumeral muscular dystrophy 1B
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facioscapulohumeral muscular dystrophy type 2
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Homo sapiens (human)
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DOID:0111194
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autosomal dominant adult-onset proximal spinal muscular atrophy
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Aliases:
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Finkel disease
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Finkel late-adult type SMA
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SMAFK
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autosomal dominant adult proximal spinal muscular atrophy
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autosomal dominant adult-onset proximal SMA
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autosomal dominant late-onset spinal muscular atrophy, Finkel type
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Mus musculus (house mouse)
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DOID:0111194
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autosomal dominant adult-onset proximal spinal muscular atrophy
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Aliases:
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Finkel disease
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Finkel late-adult type SMA
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SMAFK
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autosomal dominant adult proximal spinal muscular atrophy
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autosomal dominant adult-onset proximal SMA
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autosomal dominant late-onset spinal muscular atrophy, Finkel type
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Homo sapiens (human)
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DOID:0111196
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X-linked distal spinal muscular atrophy 3
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Aliases:
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ATP7A-related distal motor neuropathy
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DSMAX
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SMAX3
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X-linked dHMN3
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X-linked dSMA3
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X-linked distal hereditary motor neuropathy type 3
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X-linked recessive distal spinal muscular atrophy
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Mus musculus (house mouse)
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DOID:0111196
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X-linked distal spinal muscular atrophy 3
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Aliases:
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ATP7A-related distal motor neuropathy
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DSMAX
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SMAX3
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X-linked dHMN3
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X-linked dSMA3
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X-linked distal hereditary motor neuropathy type 3
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X-linked recessive distal spinal muscular atrophy
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Homo sapiens (human)
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DOID:0111196
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X-linked distal spinal muscular atrophy 3
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Aliases:
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ATP7A-related distal motor neuropathy
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DSMAX
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SMAX3
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X-linked dHMN3
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X-linked dSMA3
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X-linked distal hereditary motor neuropathy type 3
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X-linked recessive distal spinal muscular atrophy
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Rattus norvegicus (Norway rat)
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DOID:0111198
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autosomal dominant distal hereditary motor neuronopathy
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Aliases:
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autosomal dominant dHMN
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autosomal dominant distal hereditary motor neuropathy
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autosomal dominant distal spinal muscular atrophy
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Homo sapiens (human)
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DOID:0111199
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autosomal dominant distal hereditary motor neuronopathy 7
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Aliases:
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DHMN7A
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DHMNVPy
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HMN VIIA
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HMN7A
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Harper-Young myopath
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dHMN7
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distal hereditary motor neuronopathy type 7
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distal hereditary motor neuropathy type VIIA
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distal spinal muscular atrophy with vocal cord paralysis
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distal spinal muscular atrophy with vocal cord paralysis type 7A
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Mus musculus (house mouse)
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DOID:0111199
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autosomal dominant distal hereditary motor neuronopathy 7
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Aliases:
-
DHMN7A
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DHMNVPy
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HMN VIIA
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HMN7A
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Harper-Young myopath
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dHMN7
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distal hereditary motor neuronopathy type 7
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distal hereditary motor neuropathy type VIIA
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distal spinal muscular atrophy with vocal cord paralysis
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distal spinal muscular atrophy with vocal cord paralysis type 7A
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Drosophila melanogaster (fruit fly)
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DOID:0111199
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autosomal dominant distal hereditary motor neuronopathy 7
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Aliases:
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DHMN7A
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DHMNVPy
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HMN VIIA
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HMN7A
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Harper-Young myopath
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dHMN7
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distal hereditary motor neuronopathy type 7
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distal hereditary motor neuropathy type VIIA
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distal spinal muscular atrophy with vocal cord paralysis
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distal spinal muscular atrophy with vocal cord paralysis type 7A
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Homo sapiens (human)
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DOID:0111199
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autosomal dominant distal hereditary motor neuronopathy 7
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Aliases:
-
DHMN7A
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DHMNVPy
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HMN VIIA
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HMN7A
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Harper-Young myopath
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dHMN7
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distal hereditary motor neuronopathy type 7
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distal hereditary motor neuropathy type VIIA
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distal spinal muscular atrophy with vocal cord paralysis
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distal spinal muscular atrophy with vocal cord paralysis type 7A
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Rattus norvegicus (Norway rat)
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DOID:0111199
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autosomal dominant distal hereditary motor neuronopathy 7
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Aliases:
-
DHMN7A
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DHMNVPy
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HMN VIIA
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HMN7A
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Harper-Young myopath
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dHMN7
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distal hereditary motor neuronopathy type 7
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distal hereditary motor neuropathy type VIIA
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distal spinal muscular atrophy with vocal cord paralysis
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distal spinal muscular atrophy with vocal cord paralysis type 7A
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Caenorhabditis elegans
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DOID:0111202
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autosomal dominant distal hereditary motor neuronopathy 14
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Aliases:
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DHMN7B
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HMN VIIB
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HMN7B
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Harper-Young myopathy
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distal hereditary motor neuronopathy type 7B
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distal hereditary motor neuropathy type VIIB
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distal spinal muscular atrophy with vocal cord paralysis type 7B
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Mus musculus (house mouse)
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DOID:0111202
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autosomal dominant distal hereditary motor neuronopathy 14
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Aliases:
-
DHMN7B
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HMN VIIB
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HMN7B
-
Harper-Young myopathy
-
distal hereditary motor neuronopathy type 7B
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distal hereditary motor neuropathy type VIIB
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distal spinal muscular atrophy with vocal cord paralysis type 7B
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Homo sapiens (human)
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DOID:0111202
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autosomal dominant distal hereditary motor neuronopathy 14
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Aliases:
-
DHMN7B
-
HMN VIIB
-
HMN7B
-
Harper-Young myopathy
-
distal hereditary motor neuronopathy type 7B
-
distal hereditary motor neuropathy type VIIB
-
distal spinal muscular atrophy with vocal cord paralysis type 7B
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Rattus norvegicus (Norway rat)
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DOID:0111206
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autosomal dominant distal hereditary motor neuronopathy 2
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Aliases:
-
HMN II
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HMN IIA
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HMN2
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HMN2A
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autosomal dominant adult spinal muscular atrophy IIA
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distal hereditary motor neuronopathy type 2
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distal hereditary motor neuronopathy type 2A
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distal hereditary motor neuropathy type II
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distal hereditary motor neuropathy type IIA
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spinal Charcot-Marie-Tooth disease IIA
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Homo sapiens (human)
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DOID:0111206
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autosomal dominant distal hereditary motor neuronopathy 2
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Aliases:
-
HMN II
-
HMN IIA
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HMN2
-
HMN2A
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autosomal dominant adult spinal muscular atrophy IIA
-
distal hereditary motor neuronopathy type 2
-
distal hereditary motor neuronopathy type 2A
-
distal hereditary motor neuropathy type II
-
distal hereditary motor neuropathy type IIA
-
spinal Charcot-Marie-Tooth disease IIA
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Mus musculus (house mouse)
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DOID:0111206
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autosomal dominant distal hereditary motor neuronopathy 2
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Aliases:
-
HMN II
-
HMN IIA
-
HMN2
-
HMN2A
-
autosomal dominant adult spinal muscular atrophy IIA
-
distal hereditary motor neuronopathy type 2
-
distal hereditary motor neuronopathy type 2A
-
distal hereditary motor neuropathy type II
-
distal hereditary motor neuropathy type IIA
-
spinal Charcot-Marie-Tooth disease IIA
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Rattus norvegicus (Norway rat)
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