Matches in DBpedia 2015-10 for { <http://dbpedia.org/resource/Distal_spinal_muscular_atrophy_type_2> ?p ?o }
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- Distal_spinal_muscular_atrophy_type_2 abstract "Distal spinal muscular atrophy type 2 (DSMA2), also known as Jerash type distal hereditary motor neuropathy (HMN-J) — is a childhood-onset genetic disorder characterised by progressive muscle wasting affecting lower and subsequently upper limbs. The disorder has been described in Arab inhabitants of Jerash region in Jordan.The condition is linked to a genetic mutation in the locus 9p21.1–p12 (chromosome 9) and is likely inherited in an autosomal recessive manner.".
- Distal_spinal_muscular_atrophy_type_2 omim "605726".
- Distal_spinal_muscular_atrophy_type_2 wikiPageID "39885820".
- Distal_spinal_muscular_atrophy_type_2 wikiPageLength "1919".
- Distal_spinal_muscular_atrophy_type_2 wikiPageOutDegree "11".
- Distal_spinal_muscular_atrophy_type_2 wikiPageRevisionID "662848909".
- Distal_spinal_muscular_atrophy_type_2 wikiPageWikiLink Arab.
- Distal_spinal_muscular_atrophy_type_2 wikiPageWikiLink Arabs.
- Distal_spinal_muscular_atrophy_type_2 wikiPageWikiLink Autosomal_recessive.
- Distal_spinal_muscular_atrophy_type_2 wikiPageWikiLink Category:Genetic_disorders.
- Distal_spinal_muscular_atrophy_type_2 wikiPageWikiLink Category:Muscular_disorders.
- Distal_spinal_muscular_atrophy_type_2 wikiPageWikiLink Chromosome_9.
- Distal_spinal_muscular_atrophy_type_2 wikiPageWikiLink Chromosome_9_(human).
- Distal_spinal_muscular_atrophy_type_2 wikiPageWikiLink Distal_hereditary_motor_neuropathies.
- Distal_spinal_muscular_atrophy_type_2 wikiPageWikiLink Dominance_(genetics).
- Distal_spinal_muscular_atrophy_type_2 wikiPageWikiLink Jerash.
- Distal_spinal_muscular_atrophy_type_2 wikiPageWikiLink Jordan.
- Distal_spinal_muscular_atrophy_type_2 wikiPageWikiLink Locus_(genetics).
- Distal_spinal_muscular_atrophy_type_2 wikiPageWikiLink Mutation.
- Distal_spinal_muscular_atrophy_type_2 wikiPageWikiLink Spinal_muscular_atrophies.
- Distal_spinal_muscular_atrophy_type_2 wikiPageWikiLinkText "Distal spinal muscular atrophy type 2".
- Distal_spinal_muscular_atrophy_type_2 hasPhotoCollection Distal_spinal_muscular_atrophy_type_2.
- Distal_spinal_muscular_atrophy_type_2 name "Distal spinal muscular atrophy type 2".
- Distal_spinal_muscular_atrophy_type_2 omim "605726".
- Distal_spinal_muscular_atrophy_type_2 wikiPageUsesTemplate Template:About.
- Distal_spinal_muscular_atrophy_type_2 wikiPageUsesTemplate Template:Genetic-disorder-stub.
- Distal_spinal_muscular_atrophy_type_2 wikiPageUsesTemplate Template:Infobox_disease.
- Distal_spinal_muscular_atrophy_type_2 wikiPageUsesTemplate Template:Reflist.
- Distal_spinal_muscular_atrophy_type_2 subject Category:Genetic_disorders.
- Distal_spinal_muscular_atrophy_type_2 subject Category:Muscular_disorders.
- Distal_spinal_muscular_atrophy_type_2 hypernym Disorder.
- Distal_spinal_muscular_atrophy_type_2 type Disease.
- Distal_spinal_muscular_atrophy_type_2 type Thing.
- Distal_spinal_muscular_atrophy_type_2 type Q12136.
- Distal_spinal_muscular_atrophy_type_2 comment "Distal spinal muscular atrophy type 2 (DSMA2), also known as Jerash type distal hereditary motor neuropathy (HMN-J) — is a childhood-onset genetic disorder characterised by progressive muscle wasting affecting lower and subsequently upper limbs. The disorder has been described in Arab inhabitants of Jerash region in Jordan.The condition is linked to a genetic mutation in the locus 9p21.1–p12 (chromosome 9) and is likely inherited in an autosomal recessive manner.".
- Distal_spinal_muscular_atrophy_type_2 label "Distal spinal muscular atrophy type 2".
- Distal_spinal_muscular_atrophy_type_2 sameAs m.0w5bcpr.
- Distal_spinal_muscular_atrophy_type_2 sameAs Q16944450.
- Distal_spinal_muscular_atrophy_type_2 sameAs Q16944450.
- Distal_spinal_muscular_atrophy_type_2 wasDerivedFrom Distal_spinal_muscular_atrophy_type_2?oldid=662848909.
- Distal_spinal_muscular_atrophy_type_2 isPrimaryTopicOf Distal_spinal_muscular_atrophy_type_2.
- Distal_spinal_muscular_atrophy_type_2 name "Distal spinal muscular atrophy type 2".