Matches in DBpedia 2014 for { ?s <http://dbpedia.org/property/genereviewsnbk> ?o. }
- 17q21.31_microdeletion_syndrome genereviewsnbk "NBK24676".
- 3-M_syndrome genereviewsnbk "NBK1481".
- Acromicric_dysplasia genereviewsnbk "NBK11168".
- Acute_intermittent_porphyria genereviewsnbk "NBK1193".
- Adenosine_deaminase_deficiency genereviewsnbk "NBK1483".
- Adrenoleukodystrophy genereviewsnbk "NBK1315".
- Aicardi–Goutières_syndrome genereviewsnbk "NBK1475".
- Alexander_disease genereviewsnbk "NBK1172".
- Alkaptonuria genereviewsnbk "NBK1454".
- Alpha-mannosidosis genereviewsnbk "NBK1396".
- Alpha-thalassemia genereviewsnbk "NBK1435".
- Alpha_1-antitrypsin_deficiency genereviewsnbk "NBK1519".
- Alport_syndrome genereviewsnbk "NBK1207".
- Alzheimer's_disease genereviewsnbk "NBK1161".
- Andersen–Tawil_syndrome genereviewsnbk "NBK1264".
- Androgen_insensitivity_syndrome genereviewsnbk "NBK1429".
- Angelman_syndrome genereviewsnbk "NBK1144".
- Aniridia genereviewsnbk "NBK1360".
- Aortic_dissection genereviewsnbk "NBK1120".
- Argininemia genereviewsnbk "NBK1159".
- Autism genereviewsnbk "NBK1442".
- Autosomal_recessive_polycystic_kidney genereviewsnbk "NBK1326".
- Beckwith–Wiedemann_syndrome genereviewsnbk "NBK1394".
- Birt–Hogg–Dubé_syndrome genereviewsnbk "NBK1522".
- Bloom_syndrome genereviewsnbk "NBK1398".
- CADASIL_syndrome genereviewsnbk "NBK1500".
- Catecholaminergic_polymorphic_ventricular_tachycardia genereviewsnbk "NBK1289".
- Central_core_disease genereviewsnbk "NBK1391".
- Centronuclear_myopathy genereviewsnbk "NBK1432".
- Charcot–Marie–Tooth_disease genereviewsnbk "NBK1205".
- Charcot–Marie–Tooth_disease genereviewsnbk "NBK1242".
- Charcot–Marie–Tooth_disease genereviewsnbk "NBK1358".
- Charcot–Marie–Tooth_disease genereviewsnbk "NBK1374".
- Charcot–Marie–Tooth_disease genereviewsnbk "NBK1876".
- Chorea_acanthocytosis genereviewsnbk "NBK1387".
- Chronic_recurrent_multifocal_osteomyelitis genereviewsnbk "NBK1974".
- Chédiak–Higashi_syndrome genereviewsnbk "NBK5188".
- Cleidocranial_dysostosis genereviewsnbk "NBK1513".
- Cohen_syndrome genereviewsnbk "NBK1482".
- Complete_androgen_insensitivity_syndrome genereviewsnbk "NBK1429".
- Congenital_contractural_arachnodactyly genereviewsnbk "NBK1386".
- Congenital_generalized_lipodystrophy genereviewsnbk "NBK1212".
- Congenital_muscular_dystrophy genereviewsnbk "NBK1291".
- Craniosynostosis genereviewsnbk "NBK1455".
- Creatine_transporter_defect genereviewsnbk "NBK3794".
- Cutis_laxa genereviewsnbk "NBK1413".
- Cutis_laxa genereviewsnbk "NBK5200".
- Cutis_laxa genereviewsnbk "NBK5201".
- Cutis_laxa genereviewsnbk "NBK54467".
- Cyclic_neutropenia genereviewsnbk "NBK1533".
- De_Vivo_disease genereviewsnbk "NBK1430".
- Dentatorubral-pallidoluysian_atrophy genereviewsnbk "1491".
- Dilated_cardiomyopathy genereviewsnbk "NBK1119".
- Dilated_cardiomyopathy genereviewsnbk "NBK1309".
- Distal_muscular_dystrophy genereviewsnbk "NBK1303".
- Duane_syndrome genereviewsnbk "NBK1190".
- Dystonia genereviewsnbk "NBK1155".
- Dystonia genereviewsnbk "NBK1492".
- Emery–Dreifuss_muscular_dystrophy genereviewsnbk "NBK1379".
- Emery–Dreifuss_muscular_dystrophy genereviewsnbk "NBK1436".
- FG_syndrome genereviewsnbk "NBK1676".
- Fabry_disease genereviewsnbk "NBK1292".
- Facioscapulohumeral_muscular_dystrophy genereviewsnbk "NBK1443".
- Fahr's_syndrome genereviewsnbk "NBK1421".
- Familial_Mediterranean_fever genereviewsnbk "NBK1227".
- Familial_dysautonomia genereviewsnbk "NBK1180".
- Familial_hemiplegic_migraine genereviewsnbk "NBK1388".
- Feingold_syndrome genereviewsnbk "NBK7050".
- Focal_dermal_hypoplasia genereviewsnbk "NBK1543".
- Focal_facial_dermal_dysplasia genereviewsnbk "NBK1543".
- Friedreich's_ataxia genereviewsnbk "NBK1281".
- Frontotemporal_dementia genereviewsnbk "NBK1371".
- Frontotemporal_dementia genereviewsnbk "NBK1505".
- Fryns_syndrome genereviewsnbk "NBK1459".
- GM2_gangliosidoses genereviewsnbk "NBK1218".
- Galactose-1-phosphate_uridylyltransferase_deficiency genereviewsnbk "NBK1518".
- Galactose_epimerase_deficiency genereviewsnbk "51671".
- Galactosemia genereviewsnbk "NBK1518".
- Galactosemia genereviewsnbk "NBK51671".
- Gaucher's_disease genereviewsnbk "NBK1269".
- Giant_axonal_neuropathy genereviewsnbk "NBK1136".
- Glycogen_storage_disease_type_I genereviewsnbk "NBK1312".
- Glycogen_storage_disease_type_II genereviewsnbk "NBK1261".
- Glycogen_storage_disease_type_III genereviewsnbk "NBK26372".
- Glycogen_storage_disease_type_IV genereviewsnbk "NBK115333".
- Glycogen_storage_disease_type_IV genereviewsnbk "NBK5300".
- Glycogen_storage_disease_type_V genereviewsnbk "NBK1344".
- Glycogen_storage_disease_type_VI genereviewsnbk "NBK5941".
- Greig_cephalopolysyndactyly_syndrome genereviewsnbk "NBK1446".
- Guanidinoacetate_methyltransferase_deficiency genereviewsnbk "NBK3794".
- HFE_hereditary_haemochromatosis genereviewsnbk "NBK1440".
- Hemophagocytic_lymphohistiocytosis genereviewsnbk "NBK1444".
- Hepatic_veno-occlusive_disease genereviewsnbk "NBK1271".
- Hereditary_hemorrhagic_telangiectasia genereviewsnbk "NBK1351".
- Hereditary_neuralgic_amyotrophy genereviewsnbk "NBK1395".
- Holoprosencephaly genereviewsnbk "NBK1530".
- Holt–Oram_syndrome genereviewsnbk "NBK1111".
- Homocystinuria genereviewsnbk "NBK1524".
- Hunter_syndrome genereviewsnbk "NBK1274".
- Hurler_syndrome genereviewsnbk "NBK1162".