Matches in DBpedia 2014 for { ?s <http://dbpedia.org/property/genereviewsnbk> ?o. }
- Hyperekplexia genereviewsnbk "NBK1260".
- Hyperkalemic_periodic_paralysis genereviewsnbk "NBK1496".
- Hypochondroplasia genereviewsnbk "NBK1477".
- Hypohidrotic_ectodermal_dysplasia genereviewsnbk "NBK1112".
- Hypokalemic_periodic_paralysis genereviewsnbk "NBK1338".
- I-cell_disease genereviewsnbk "NBK1828".
- IPEX_syndrome genereviewsnbk "NBK1118".
- Inclusion_body_myositis genereviewsnbk "NBK1262".
- Incontinentia_pigmenti genereviewsnbk "NBK1472".
- Infantile_neuroaxonal_dystrophy genereviewsnbk "NBK1675".
- Infantile_systemic_hyalinosis genereviewsnbk "NBK1525".
- Jervell_and_Lange-Nielsen_syndrome genereviewsnbk "NBK1405".
- Junctional_epidermolysis_bullosa_(medicine) genereviewsnbk "NBK1125".
- Juvenile_hemochromatosis genereviewsnbk "NBK1170".
- Juvenile_polyposis_syndrome genereviewsnbk "NBK1469".
- Kearns–Sayre_syndrome genereviewsnbk "NBK1203".
- Leber's_congenital_amaurosis genereviewsnbk "NBK1298".
- Lesch–Nyhan_syndrome genereviewsnbk "NBK1149".
- Leukoencephalopathy_with_vanishing_white_matter genereviewsnbk "NBK1258".
- Leukoencephalopathy_with_vanishing_white_matter genereviewsnbk "NBK1500".
- Leukoencephalopathy_with_vanishing_white_matter genereviewsnbk "NBK32533".
- Limb-girdle_muscular_dystrophy genereviewsnbk "NBK1303".
- Limb-girdle_muscular_dystrophy genereviewsnbk "NBK1313".
- Limb-girdle_muscular_dystrophy genereviewsnbk "NBK1408".
- Lipoprotein_lipase_deficiency genereviewsnbk "NBK1308".
- Lissencephaly genereviewsnbk "NBK1185".
- Lissencephaly genereviewsnbk "NBK5189".
- Loeys–Dietz_syndrome genereviewsnbk "NBK1133".
- Lujan–Fryns_syndrome genereviewsnbk "NBK1676".
- Lymphedema–distichiasis_syndrome genereviewsnbk "NBK1457".
- Léri–Weill_dyschondrosteosis genereviewsnbk "NBK1215".
- MASA_syndrome genereviewsnbk "NBK1484".
- MERRF_syndrome genereviewsnbk "NBK1520".
- Malignant_hyperthermia genereviewsnbk "NBK1146".
- Marfan_syndrome genereviewsnbk "NBK1335".
- Marinesco–Sjögren_syndrome genereviewsnbk "NBK1192".
- McKusick–Kaufman_syndrome genereviewsnbk "NBK1502".
- McLeod_syndrome genereviewsnbk "NBK1354".
- Megalencephalic_leukoencephalopathy_with_subcortical_cysts genereviewsnbk "NBK1535".
- Membranoproliferative_glomerulonephritis genereviewsnbk "NBK1425".
- Microphthalmia genereviewsnbk "NBK1378".
- Microphthalmia–dermal_aplasia–sclerocornea_syndrome genereviewsnbk "NBK7041".
- Mild_androgen_insensitivity_syndrome genereviewsnbk "NBK1429".
- Milroy's_disease genereviewsnbk "NBK1239".
- Mitochondrial_neurogastrointestinal_encephalopathy_syndrome genereviewsnbk "NBK1179".
- Mucolipidosis_type_IV genereviewsnbk "NBK1214".
- Muenke_syndrome genereviewsnbk "NBK1415".
- Multiple_endocrine_neoplasia_type_2 genereviewsnbk "NBK1257".
- Multiple_epiphyseal_dysplasia genereviewsnbk "NBK1123".
- Multiple_epiphyseal_dysplasia genereviewsnbk "NBK1306".
- Multiple_sclerosis genereviewsnbk "NBK1316".
- Myoclonic_dystonia genereviewsnbk "NBK1414".
- Myotonic_dystrophy genereviewsnbk "NBK1165".
- Myotonic_dystrophy genereviewsnbk "NBK1466".
- Nemaline_myopathy genereviewsnbk "NBK1288".
- Nephrogenic_diabetes_insipidus genereviewsnbk "NBK1177".
- Neurofibromatosis_type_I genereviewsnbk "NBK1109".
- Neurofibromatosis_type_I genereviewsnbk "NBK47312".
- Neurofibromatosis_type_II genereviewsnbk "NBK1201".
- Niemann–Pick_disease genereviewsnbk "NBK1296".
- Niemann–Pick_disease genereviewsnbk "NBK1370".
- Niemann–Pick_disease,_SMPD1-associated genereviewsnbk "NBK1370".
- Niemann–Pick_disease,_type_C genereviewsnbk "NBK1296".
- Oculocerebrorenal_syndrome genereviewsnbk "NBK1480".
- Oculocutaneous_albinism genereviewsnbk "NBK1166".
- Oculocutaneous_albinism genereviewsnbk "NBK1232".
- Oculocutaneous_albinism genereviewsnbk "NBK1510".
- Oculopharyngeal_muscular_dystrophy genereviewsnbk "NBK1126".
- Ondine's_curse genereviewsnbk "NBK1427".
- Pantothenate_kinase-associated_neurodegeneration genereviewsnbk "NBK1490".
- Parkinson's_disease genereviewsnbk "NBK1223".
- Partial_androgen_insensitivity_syndrome genereviewsnbk "NBK1429".
- Pearson_syndrome genereviewsnbk "NBK1203".
- Pendred_syndrome genereviewsnbk "NBK1467".
- Permanent_neonatal_diabetes_mellitus genereviewsnbk "NBK1447".
- Peutz–Jeghers_syndrome genereviewsnbk "NBK1266".
- Polymicrogyria genereviewsnbk "NBK1329".
- Prader–Willi_syndrome genereviewsnbk "NBK1330".
- Progeria genereviewsnbk "NBK1121".
- Progressive_familial_intrahepatic_cholestasis genereviewsnbk "NBK1297".
- Retinitis_pigmentosa genereviewsnbk "NBK1417".
- Retinoblastoma genereviewsnbk "NBK1452".
- Rett_syndrome genereviewsnbk "NBK1497".
- Roberts_syndrome genereviewsnbk "NBK1153".
- Rubinstein–Taybi_syndrome genereviewsnbk "NBK1526".
- Salla_disease genereviewsnbk "NBK1470".
- Silver–Russell_syndrome genereviewsnbk "NBK1324".
- Spinal_muscular_atrophy genereviewsnbk "NBK1352".
- Thalassemia genereviewsnbk "NBK1426".
- Thalassemia genereviewsnbk "NBK1435".
- Thyrotoxic_periodic_paralysis genereviewsnbk "NBK1338".
- Transient_neonatal_diabetes_mellitus genereviewsnbk "NBK1534".
- Trimethylaminuria genereviewsnbk "NBK1103".
- Ullrich_congenital_muscular_dystrophy genereviewsnbk "NBK1503".
- Von_Hippel–Lindau_disease genereviewsnbk "NBK1463".
- Von_Willebrand_disease genereviewsnbk "NBK7014".
- Werner_syndrome genereviewsnbk "NBK1514".
- Wilson's_disease genereviewsnbk "NBK1512".
- X-linked_lymphoproliferative_disease genereviewsnbk "NBK1406".
- X-linked_recessive_chondrodysplasia_punctata genereviewsnbk "NBK1544".