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- Distal_hereditary_motor_neuronopathies abstract "Distal hereditary motor neuronopathies (distal HMN, dHMN), sometimes also called distal hereditary motor neuropathies, are a genetically and clinically heterogeneous group of motor neuron diseases that result from genetic mutations in various genes and are characterized by degeneration and loss of motor neuron cells in the anterior horn of the spinal cord and subsequent muscle atrophy.Although they can hardly be distinguished from hereditary motor and sensory neuropathies on the clinical level, dHMNs are considered a separate class of disorders.".
- Distal_hereditary_motor_neuronopathies wikiPageID "34389965".
- Distal_hereditary_motor_neuronopathies wikiPageLength "4821".
- Distal_hereditary_motor_neuronopathies wikiPageOutDegree "63".
- Distal_hereditary_motor_neuronopathies wikiPageRevisionID "687217503".
- Distal_hereditary_motor_neuronopathies wikiPageWikiLink Anterior_grey_column.
- Distal_hereditary_motor_neuronopathies wikiPageWikiLink Atrophy.
- Distal_hereditary_motor_neuronopathies wikiPageWikiLink Autosomal_dominant_distal_spinal_muscular_atrophy.
- Distal_hereditary_motor_neuronopathies wikiPageWikiLink Autosomal_dominant_juvenile_distal_spinal_muscular_atrophy.
- Distal_hereditary_motor_neuronopathies wikiPageWikiLink Category:Motor_neurone_disease.
- Distal_hereditary_motor_neuronopathies wikiPageWikiLink Charcot–Marie–Tooth_disease.
- Distal_hereditary_motor_neuronopathies wikiPageWikiLink Choline_transporter.
- Distal_hereditary_motor_neuronopathies wikiPageWikiLink Chromosome_11_(human).
- Distal_hereditary_motor_neuronopathies wikiPageWikiLink Chromosome_12_(human).
- Distal_hereditary_motor_neuronopathies wikiPageWikiLink Chromosome_2_(human).
- Distal_hereditary_motor_neuronopathies wikiPageWikiLink Chromosome_5_(human).
- Distal_hereditary_motor_neuronopathies wikiPageWikiLink Chromosome_7_(human).
- Distal_hereditary_motor_neuronopathies wikiPageWikiLink Chromosome_9_(human).
- Distal_hereditary_motor_neuronopathies wikiPageWikiLink DCTN1.
- Distal_hereditary_motor_neuronopathies wikiPageWikiLink Distal_spinal_muscular_atrophy_type_1.
- Distal_hereditary_motor_neuronopathies wikiPageWikiLink Distal_spinal_muscular_atrophy_type_2.
- Distal_hereditary_motor_neuronopathies wikiPageWikiLink Distal_spinal_muscular_atrophy_type_3.
- Distal_hereditary_motor_neuronopathies wikiPageWikiLink Distal_spinal_muscular_atrophy_type_VA.
- Distal_hereditary_motor_neuronopathies wikiPageWikiLink Distal_spinal_muscular_atrophy_type_VB.
- Distal_hereditary_motor_neuronopathies wikiPageWikiLink Distal_spinal_muscular_atrophy_with_calf_predominance.
- Distal_hereditary_motor_neuronopathies wikiPageWikiLink Dominance_(genetics).
- Distal_hereditary_motor_neuronopathies wikiPageWikiLink FBXO38.
- Distal_hereditary_motor_neuronopathies wikiPageWikiLink Gene.
- Distal_hereditary_motor_neuronopathies wikiPageWikiLink Glycine—tRNA_ligase.
- Distal_hereditary_motor_neuronopathies wikiPageWikiLink HSPB3.
- Distal_hereditary_motor_neuronopathies wikiPageWikiLink HSPB8.
- Distal_hereditary_motor_neuronopathies wikiPageWikiLink Hereditary_motor_and_sensory_neuropathy.
- Distal_hereditary_motor_neuronopathies wikiPageWikiLink Hereditary_spastic_paraplegia.
- Distal_hereditary_motor_neuronopathies wikiPageWikiLink Hsp27.
- Distal_hereditary_motor_neuronopathies wikiPageWikiLink IGHMBP2.
- Distal_hereditary_motor_neuronopathies wikiPageWikiLink Inheritance.
- Distal_hereditary_motor_neuronopathies wikiPageWikiLink Locus_(genetics).
- Distal_hereditary_motor_neuronopathies wikiPageWikiLink Motor_neuron.
- Distal_hereditary_motor_neuronopathies wikiPageWikiLink Motor_neuron_disease.
- Distal_hereditary_motor_neuronopathies wikiPageWikiLink Mutation.
- Distal_hereditary_motor_neuronopathies wikiPageWikiLink Online_Mendelian_Inheritance_in_Man.
- Distal_hereditary_motor_neuronopathies wikiPageWikiLink REEP1.
- Distal_hereditary_motor_neuronopathies wikiPageWikiLink Spinal_muscular_atrophies.
- Distal_hereditary_motor_neuronopathies wikiPageWikiLink Spinal_muscular_atrophy_with_vocal_cord_paralysis.
- Distal_hereditary_motor_neuronopathies wikiPageWikiLinkText "Distal hereditary motor neuronopathies".
- Distal_hereditary_motor_neuronopathies wikiPageWikiLinkText "distal hereditary motor neuropathy".
- Distal_hereditary_motor_neuronopathies wikiPageUsesTemplate Template:OMIM2.
- Distal_hereditary_motor_neuronopathies subject Category:Motor_neurone_disease.
- Distal_hereditary_motor_neuronopathies type Disorder.
- Distal_hereditary_motor_neuronopathies comment "Distal hereditary motor neuronopathies (distal HMN, dHMN), sometimes also called distal hereditary motor neuropathies, are a genetically and clinically heterogeneous group of motor neuron diseases that result from genetic mutations in various genes and are characterized by degeneration and loss of motor neuron cells in the anterior horn of the spinal cord and subsequent muscle atrophy.Although they can hardly be distinguished from hereditary motor and sensory neuropathies on the clinical level, dHMNs are considered a separate class of disorders.".
- Distal_hereditary_motor_neuronopathies label "Distal hereditary motor neuronopathies".
- Distal_hereditary_motor_neuronopathies sameAs Q5282840.
- Distal_hereditary_motor_neuronopathies sameAs m.0h_cbjr.
- Distal_hereditary_motor_neuronopathies sameAs Q5282840.
- Distal_hereditary_motor_neuronopathies wasDerivedFrom Distal_hereditary_motor_neuronopathies?oldid=687217503.
- Distal_hereditary_motor_neuronopathies isPrimaryTopicOf Distal_hereditary_motor_neuronopathies.