Matches in DBpedia 2014 for { ?s <http://dbpedia.org/property/genereviewsname> ?o. }
- Hypochondroplasia genereviewsname "Hypochondroplasia".
- Hypogonadism genereviewsname "Isolated Gonadotropin-Releasing Hormone Deficiency Overview".
- Hypohidrotic_ectodermal_dysplasia genereviewsname "Hypohidrotic Ectodermal Dysplasia".
- Hypokalemic_periodic_paralysis genereviewsname "Hypokalemic Periodic Paralysis".
- I-cell_disease genereviewsname "Mucolipidosis II".
- IPEX_syndrome genereviewsname "IPEX Syndrome".
- Inclusion_body_myositis genereviewsname "Inclusion Body Myopathy 2".
- Incontinentia_pigmenti genereviewsname "Incontinentia pigmenti".
- Infantile_neuroaxonal_dystrophy genereviewsname "PLA2G6-Associated Neurodegeneration".
- Infantile_systemic_hyalinosis genereviewsname "Hyalinosis, Inherited Systemic".
- Jervell_and_Lange-Nielsen_syndrome genereviewsname "Jervell and Lange-Nielsen Syndrome".
- Junctional_epidermolysis_bullosa_(medicine) genereviewsname "Junctional Epidermolysis Bullosa".
- Juvenile_hemochromatosis genereviewsname "Juvenile Hereditary Hemochromatosis".
- Juvenile_polyposis_syndrome genereviewsname "Juvenile Polyposis Syndrome".
- Kearns–Sayre_syndrome genereviewsname "Mitochondrial DNA Deletion Syndromes".
- Leber's_congenital_amaurosis genereviewsname "Leber Congenital Amaurosis".
- Lesch–Nyhan_syndrome genereviewsname "Lesch-Nyhan Syndrome".
- Leukoencephalopathy_with_vanishing_white_matter genereviewsname "CADASIL".
- Leukoencephalopathy_with_vanishing_white_matter genereviewsname "CARASIL Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy, Maeda Syndrome".
- Leukoencephalopathy_with_vanishing_white_matter genereviewsname "Childhood Ataxia with Central Nervous System Hypomylenation/Vanishing White Matter".
- Limb-girdle_muscular_dystrophy genereviewsname "Calpainopathy".
- Limb-girdle_muscular_dystrophy genereviewsname "Dysferlinopathy".
- Limb-girdle_muscular_dystrophy genereviewsname "Limb-Girdle Muscular Dystrophy Overview".
- Lipoprotein_lipase_deficiency genereviewsname "Familial Lipoprotein Lipase Deficiency".
- Lissencephaly genereviewsname "DCX-Related Disorders".
- Lissencephaly genereviewsname "LIS1-Associated Lissencephaly/Subcortical Band Heterotopia".
- Loeys–Dietz_syndrome genereviewsname "Loeys-Dietz Syndrome".
- Lujan–Fryns_syndrome genereviewsname "MED12-Related Disorders".
- Lymphedema–distichiasis_syndrome genereviewsname "Lymphedema-Distichiasis Syndrome".
- Léri–Weill_dyschondrosteosis genereviewsname "SHOX-Related Haploinsufficiency Disorders".
- MASA_syndrome genereviewsname "L1 Syndrome".
- MERRF_syndrome genereviewsname "MERRF".
- Malignant_hyperthermia genereviewsname "Malignant Hyperthermia Susceptibility".
- Marfan_syndrome genereviewsname "Marfan Syndrome".
- Marinesco–Sjögren_syndrome genereviewsname "Marinesco-Sjögren Syndrome".
- McKusick–Kaufman_syndrome genereviewsname "McKusick-Kaufman Syndrome".
- McLeod_syndrome genereviewsname "McLeod Neuroacanthocytosis Syndrome".
- Megalencephalic_leukoencephalopathy_with_subcortical_cysts genereviewsname "Megalencephalic Leukoencephalopathy with Subcortical Cysts".
- Membranoproliferative_glomerulonephritis genereviewsname "Dense Deposit Disease/Membranoproliferative Glomerulonephritis Type II".
- Microphthalmia genereviewsname "Anophthalmia / Microphthalmia Overview".
- Microphthalmia–dermal_aplasia–sclerocornea_syndrome genereviewsname "Microphthalmia with Linear Skin Defects Syndrome".
- Mild_androgen_insensitivity_syndrome genereviewsname "Androgen Insensitivity Syndrome".
- Milroy's_disease genereviewsname "Milroy Disease".
- Mitochondrial_neurogastrointestinal_encephalopathy_syndrome genereviewsname "Mitochondrial Neurogastrointestinal Encephalopathy Disease".
- Mucolipidosis_type_IV genereviewsname "Mucolipidosis IV".
- Muenke_syndrome genereviewsname "Muenke Syndrome".
- Multiple_endocrine_neoplasia_type_2 genereviewsname "Multiple Endocrine Neoplasia Type 2".
- Multiple_epiphyseal_dysplasia genereviewsname "Multiple Epiphyseal Dysplasia, Dominant".
- Multiple_epiphyseal_dysplasia genereviewsname "Multiple Epiphyseal Dysplasia, Recessive".
- Multiple_sclerosis genereviewsname "Overview".
- Myoclonic_dystonia genereviewsname "Myoclonus-Dystonia".
- Myotonic_dystrophy genereviewsname "Myotonic Dystrophy Type 1".
- Myotonic_dystrophy genereviewsname "Myotonic Dystrophy Type 2".
- Nemaline_myopathy genereviewsname "Nemaline myopathy".
- Nephrogenic_diabetes_insipidus genereviewsname "Nephrogenic Diabetes Insipidus".
- Neurofibromatosis_type_I genereviewsname "Legius Syndrome".
- Neurofibromatosis_type_I genereviewsname "Neurofibromatosis 1".
- Neurofibromatosis_type_II genereviewsname "Neurofibromatosis 2".
- Niemann–Pick_disease genereviewsname "Acid Sphingomyelinase Deficiency — includes: Niemann–Pick Disease Type A, B".
- Niemann–Pick_disease genereviewsname "Niemann-Pick Disease Type C".
- Niemann–Pick_disease,_SMPD1-associated genereviewsname "Acid Sphingomyelinase Deficiency".
- Niemann–Pick_disease,_type_C genereviewsname "Niemann-Pick Disease Type C".
- Oculocerebrorenal_syndrome genereviewsname "Lowe Syndrome".
- Oculocutaneous_albinism genereviewsname "Oculocutaneous Albinism Type 1".
- Oculocutaneous_albinism genereviewsname "Oculocutaneous Albinism Type 2".
- Oculocutaneous_albinism genereviewsname "Oculocutaneous Albinism Type 4".
- Oculopharyngeal_muscular_dystrophy genereviewsname "Oculopharyngeal Muscular Dystrophy".
- Ondine's_curse genereviewsname "Congenital Central Hypoventilation Syndrome".
- Pantothenate_kinase-associated_neurodegeneration genereviewsname "Pantothenate Kinase-Associated Neurodegeneration".
- Parkinson's_disease genereviewsname "Parkinson Disease Overview".
- Partial_androgen_insensitivity_syndrome genereviewsname "Androgen Insensitivity Syndrome".
- Pearson_syndrome genereviewsname "Mitochondrial DNA Deletion Syndromes".
- Pendred_syndrome genereviewsname "Pendred Syndrome/DFNB4".
- Permanent_neonatal_diabetes_mellitus genereviewsname "Permanent Neonatal Diabetes Mellitus".
- Peutz–Jeghers_syndrome genereviewsname "Peutz-Jeghers Syndrome".
- Polymicrogyria genereviewsname "Polymicrogyria Overview".
- Prader–Willi_syndrome genereviewsname "Prader-Willi Syndrome".
- Progeria genereviewsname "Hutchinson-Gilford Progeria Syndrome".
- Progressive_familial_intrahepatic_cholestasis genereviewsname "Low γ-GT Familial Intrahepatic Cholestasis".
- Retinitis_pigmentosa genereviewsname "Retinitis Pigmentosa Overview".
- Retinoblastoma genereviewsname "Retinoblastoma".
- Rett_syndrome genereviewsname "MECP2-Related Disorders".
- Roberts_syndrome genereviewsname "Roberts syndrome".
- Rubinstein–Taybi_syndrome genereviewsname "Rubinstein–Taybi syndrome".
- Salla_disease genereviewsname "Free Sialic Acid Storage Disorders".
- Sickle-cell_disease genereviewsname "Sickle-cell disease".
- Silver–Russell_syndrome genereviewsname "Russell-Silver Syndrome".
- Spinal_muscular_atrophy genereviewsname "Spinal Muscular Atrophy".
- Thalassemia genereviewsname "Alpha-Thalassemia".
- Thalassemia genereviewsname "Beta-Thalassemia".
- Thyrotoxic_periodic_paralysis genereviewsname "Hypokalemic Periodic Paralysis".
- Transient_neonatal_diabetes_mellitus genereviewsname "Diabetes Mellitus, 6q24-Related Transient Neonatal".
- Trimethylaminuria genereviewsname "Trimethylaminuria".
- Ullrich_congenital_muscular_dystrophy genereviewsname "Collagen Type VI-Related Disorders".
- Von_Hippel–Lindau_disease genereviewsname "Von Hippel-Lindau Syndrome".
- Von_Willebrand_disease genereviewsname "von Willebrand Disease".
- Werner_syndrome genereviewsname "Werner Syndrome".
- Wilson's_disease genereviewsname "Wilson Disease".
- X-linked_lymphoproliferative_disease genereviewsname "Lymphoproliferative Disease, X-Linked".
- X-linked_recessive_chondrodysplasia_punctata genereviewsname "Chondrodysplasia Punctata 1, X-Linked Recessive".