Matches in DBpedia 2014 for { ?s <http://dbpedia.org/property/genereviewsname> ?o. }
- 17q21.31_microdeletion_syndrome genereviewsname "17".
- 3-M_syndrome genereviewsname "3".
- Acromicric_dysplasia genereviewsname "Geleophysic Dysplasia".
- Acute_intermittent_porphyria genereviewsname "Hydroxymethylbilane Synthase Deficiency".
- Adenosine_deaminase_deficiency genereviewsname "Adenosine Deaminase Deficiency".
- Adrenoleukodystrophy genereviewsname "X-Linked Adrenoleukodystrophy".
- Aicardi–Goutières_syndrome genereviewsname "Aicardi–Goutières Syndrome".
- Alexander_disease genereviewsname "Alexander disease".
- Alkaptonuria genereviewsname "Alkaptonuria".
- Alpha-mannosidosis genereviewsname "Alpha-Mannosidosis".
- Alpha-thalassemia genereviewsname "Alpha-Thalassemia".
- Alpha_1-antitrypsin_deficiency genereviewsname "Alpha1-Antitrypsin Deficiency".
- Alport_syndrome genereviewsname "Collagen IV-Related Nephropathies".
- Andersen–Tawil_syndrome genereviewsname "Andersen-Tawil syndrome".
- Androgen_insensitivity_syndrome genereviewsname "Androgen Insensitivity Syndrome".
- Angelman_syndrome genereviewsname "Angelman Syndrome".
- Aniridia genereviewsname "Aniridia".
- Aortic_dissection genereviewsname "Thoracic Aortic Aneurysms and Aortic Dissections".
- Argininemia genereviewsname "Arginase Deficiency".
- Autism genereviewsname "Autism overview".
- Autosomal_recessive_polycystic_kidney genereviewsname "Polycystic Kidney Disease, Autosomal Recessive".
- Beckwith–Wiedemann_syndrome genereviewsname "Beckwith-Wiedemann Syndrome".
- Birt–Hogg–Dubé_syndrome genereviewsname "Birt-Hogg-Dubé Syndrome".
- Bloom_syndrome genereviewsname "Bloom's Syndrome".
- CADASIL_syndrome genereviewsname "CADASIL".
- Centronuclear_myopathy genereviewsname "X-Linked Centronuclear Myopathy".
- Charcot–Marie–Tooth_disease genereviewsname "Charcot-Marie-Tooth Hereditary Neuropathy Overview".
- Charcot–Marie–Tooth_disease genereviewsname "Charcot-Marie-Tooth Neuropathy Type 1".
- Charcot–Marie–Tooth_disease genereviewsname "Charcot-Marie-Tooth Neuropathy X Type 1".
- Charcot–Marie–Tooth_disease genereviewsname "Charcot-Marie-Tooth Neuropathy X Type 5".
- Charcot–Marie–Tooth_disease genereviewsname "GARS-Associated Axonal Neuropathy, Charcot-Marie-Tooth Neuropathy Type 2D, Distal Spinal Muscular Atrophy V".
- Chorea_acanthocytosis genereviewsname "Choreoacanthocytosis".
- Chronic_recurrent_multifocal_osteomyelitis genereviewsname "Majeed Syndrome".
- Chédiak–Higashi_syndrome genereviewsname "Chediak-Higashi Syndrome".
- Cleidocranial_dysostosis genereviewsname "Cleidocranial Dysplasia".
- Coeliac_disease genereviewsname "Celiac Disease".
- Cohen_syndrome genereviewsname "Cohen Syndrome".
- Complete_androgen_insensitivity_syndrome genereviewsname "Androgen Insensitivity Syndrome".
- Congenital_contractural_arachnodactyly genereviewsname "Congenital Contractural Arachnodactyly".
- Congenital_generalized_lipodystrophy genereviewsname "Berardinelli-Seip Congenital Lipodystrophy".
- Congenital_muscular_dystrophy genereviewsname "Congenital Muscular Dystrophy Overview".
- Craniosynostosis genereviewsname "FGFR-Related Craniosynostosis Syndromes".
- Creatine_transporter_defect genereviewsname "Creatine Deficiency Syndromes".
- Cutis_laxa genereviewsname "ATP6V0A2-Related Cutis Laxa".
- Cutis_laxa genereviewsname "ATP7A-Related Copper Transport Disorders".
- Cutis_laxa genereviewsname "EFEMP2-Related Cutis Laxa".
- Cutis_laxa genereviewsname "FBLN5-Related Cutis Laxa".
- Cyclic_neutropenia genereviewsname "ELANE-Related Neutropenia".
- De_Vivo_disease genereviewsname "Glucose Transporter Type 1 Deficiency Syndrome".
- Dentatorubral-pallidoluysian_atrophy genereviewsname "DRPLA".
- Dilated_cardiomyopathy genereviewsname "Dilated Cardiomyopathy Overview".
- Dilated_cardiomyopathy genereviewsname "Dystrophinopathies".
- Distal_muscular_dystrophy genereviewsname "Dysferlinopathy".
- Duane_syndrome genereviewsname "Duane Syndrome".
- Dystonia genereviewsname "Dystonia Overview".
- Dystonia genereviewsname "Early-Onset Primary Dystonia".
- Emery–Dreifuss_muscular_dystrophy genereviewsname "Emery-Dreifuss Muscular Dystrophy".
- Emery–Dreifuss_muscular_dystrophy genereviewsname "SYNE1-Related Autosomal Recessive Cerebellar Ataxia".
- FG_syndrome genereviewsname "MED12-related disorders".
- Fabry_disease genereviewsname "Fabry disease".
- Facioscapulohumeral_muscular_dystrophy genereviewsname "Facioscapulohumeral muscular dystrophy".
- Fahr's_syndrome genereviewsname "Familial Idiopathic Basal Ganglia Calcification".
- Familial_Mediterranean_fever genereviewsname "Familial Mediterranean Fever".
- Familial_dysautonomia genereviewsname "Familial dysautonomia".
- Familial_hemiplegic_migraine genereviewsname "Familial Hemiplegic Migraine".
- Feingold_syndrome genereviewsname "Feingold Syndrome 1".
- Focal_dermal_hypoplasia genereviewsname "Focal Dermal Hypoplasia".
- Focal_facial_dermal_dysplasia genereviewsname "Focal Dermal Hypoplasia".
- Friedreich's_ataxia genereviewsname "Friedreich Ataxia".
- Frontotemporal_dementia genereviewsname "GRN-Related Frontotemporal Dementia".
- Frontotemporal_dementia genereviewsname "MAPT-Related Disorders".
- Fryns_syndrome genereviewsname "Fryns syndrome".
- GM2_gangliosidoses genereviewsname "Hexosaminidase A Deficiency".
- Galactose-1-phosphate_uridylyltransferase_deficiency genereviewsname "Galactosemia".
- Galactose_epimerase_deficiency genereviewsname "Epimerase Deficiency Galactosemia".
- Galactosemia genereviewsname "Epimerase Deficiency Galactosemia".
- Galactosemia genereviewsname "Galactosemia".
- Gaucher's_disease genereviewsname "Gaucher Disease".
- Giant_axonal_neuropathy genereviewsname "Giant Axonal Neuropathy".
- Glycogen_storage_disease_type_I genereviewsname "Glycogen Storage Disease Type I".
- Glycogen_storage_disease_type_II genereviewsname "Glycogen Storage Disease Type II".
- Glycogen_storage_disease_type_III genereviewsname "Glycogen Storage Disease Type III".
- Glycogen_storage_disease_type_IV genereviewsname "Adult Polyglucosan Body Disease".
- Glycogen_storage_disease_type_IV genereviewsname "Glycogen Storage Disease Type IV".
- Glycogen_storage_disease_type_V genereviewsname "Glycogen Storage Disease Type V".
- Glycogen_storage_disease_type_VI genereviewsname "Glycogen Storage Disease Type VI".
- Greig_cephalopolysyndactyly_syndrome genereviewsname "Greig Cephalopolysyndactyly Syndrome".
- Guanidinoacetate_methyltransferase_deficiency genereviewsname "Creatine Deficiency Syndromes".
- HFE_hereditary_haemochromatosis genereviewsname "HFE-Associated Hereditary Hemochromatosis".
- Hemophagocytic_lymphohistiocytosis genereviewsname "Familial Hemophagocytic Lymphohistiocytosis".
- Hepatic_veno-occlusive_disease genereviewsname "Venous Occlusive Disease with Immunodeficiency".
- Hereditary_hemorrhagic_telangiectasia genereviewsname "Hereditary Hemorrhagic Telangiectasia".
- Hereditary_neuralgic_amyotrophy genereviewsname "Hereditary Neuralgic Amyotrophy".
- Holoprosencephaly genereviewsname "Holoprosencephaly Overview".
- Holt–Oram_syndrome genereviewsname "Holt-Oram Syndrome".
- Homocystinuria genereviewsname "Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency".
- Hunter_syndrome genereviewsname "Mucopolysaccharidosis Type II".
- Hurler_syndrome genereviewsname "Mucopolysaccharidosis Type I".
- Hyperekplexia genereviewsname "Hyperekplexia".
- Hyperkalemic_periodic_paralysis genereviewsname "Hyperkalemic Periodic Paralysis Type 1".