Matches in DBpedia 2016-04 for { ?s <http://dbpedia.org/property/omimMult> ?o }
Showing triples 1 to 14 of
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- Albinism omimMult ", , , , , , , , , , , , , , , , , , , ,".
- Complement_deficiency omimMult ", ,".
- GM1_gangliosidoses omimMult ",".
- GM2_gangliosidoses omimMult ",".
- Galactosemia omimMult "Epimerase Deficiency Galactosemia".
- Hereditary_spastic_paraplegia omimMult PS303350.
- Hypohidrotic_ectodermal_dysplasia omimMult ",".
- Leukoencephalopathy_with_vanishing_white_matter omimMult "CARASIL: CADASIL:".
- Neurofibromatosis omimMult ",".
- Pemphigus omimMult "Benign Chronic ~".
- Pemphigus omimMult "~ Vulgaris, Familial".
- Terminal_complement_pathway_deficiency omimMult ", ,".
- XX_gonadal_dysgenesis omimMult "Perrault syndrome".
- XX_gonadal_dysgenesis omimMult "XX gonadal dysgenesis".