About: Progeroid syndromes

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Range of genetic disorders which cause a person to appear to grow older faster

Property	Value
dbo:description	مجموعة من الاضطرابات الجينية (ar) range of genetic disorders which cause a person to appear to grow older faster (en)
dbo:thumbnail	wiki-commons:Special:FilePath/Autosomal_recessive_-_en.svg?width=300
dbo:wikiPageExternalLink	http://rarediseases.info.nih.gov/ https://www.ncbi.nlm.nih.gov/books/NBK1121/ http://www.orpha.net
dbo:wikiPageWikiLink	dbr:Macrocephaly dbr:HELLP_syndrome dbr:Calcinosis dbr:Ageing dbr:Dean_Koontz dbr:Lamin dbr:Rothmund–Thomson_syndrome dbr:Dysmorphic_feature dbr:Charles_Dickens dbr:Yui_(singer) dbr:Lung_cancer dbr:Robin_Williams dbr:Stem_cell dbr:Translation_(biology) dbr:Mitosis dbr:Congenital dbr:Frameshift_mutation dbr:Non-homologous_end_joining dbr:Senescence dbr:Sister_chromatids dbr:Genome_instability dbr:Alzheimer's_disease dbc:Aging-associated_diseases dbc:Genetic_diseases_and_disorders dbr:Deafness dbr:Diabetes dbr:Ultraviolet dbr:Ashkenazi_Jews dbr:Cataract dbr:Fertility dbr:Gastroesophageal_reflux_disease dbr:Osteoporosis dbr:Deamination dbr:Preterm_birth dbr:Moonlight_Bay_Trilogy dbr:Nestor-Guillermo_progeria_syndrome dbr:Exon dbr:Cardiovascular_disease dbr:National_Institutes_of_Health dbr:Microcephaly dbc:Progeroid_syndromes dbr:Xeroderma_pigmentosum dbr:Nonsense_mutation dbr:Chaos;Head dbr:Nucleotide_excision_repair dbr:Red_eye_(medicine) dbr:Phenotype dbr:DNA_ligase dbr:Regulation_of_gene_expression dbr:Ubiquitin dbr:Otitis dbr:Sunburn dbr:Depurination dbr:Werner_syndrome dbc:Senescence dbr:Denmark dbr:Physiology dbr:Sulfur dbr:Atrophy dbr:DNA_damage_theory_of_aging dbr:Regeneration_(biology) dbr:Skin_cancer dbr:DNA_repair dbr:Genetic_recombination dbr:Gonad dbr:Progeria dbr:Brain_tumor dbr:Failure_to_thrive dbr:Malignancy dbr:Placenta dbr:Genodermatosis dbr:Entropion dbr:Scleroderma dbr:Aquiline_nose dbr:Birth_weight dbr:Progerin dbr:Gene dbr:Genetic_disorder dbr:Pathology dbr:Pre-eclampsia dbr:Uterus dbc:Rare_syndromes dbr:Infertility dbr:Menopause dbr:Ichthyosis dbr:Nijmegen_breakage_syndrome dbr:Photosensitivity_in_humans dbr:Type_2_diabetes dbr:Radiation dbr:Cell_nucleus dbr:Adenosine_triphosphate dbr:F._Scott_Fitzgerald dbr:DNA_replication dbr:Apoptosis dbr:ERCC2 dbr:Reactive_oxygen_species dbr:XPB dbr:Cell_culture dbr:Centromere dbr:Freckle dbr:Li–Fraumeni_syndrome dbr:Messenger_RNA dbr:Dyskeratosis_congenita dbr:Upper_respiratory_tract_infection dbr:DeSanctis–Cacchione_syndrome dbr:Vasodilation dbr:Amitabh_Bachchan dbr:Cancer dbr:Chronic_obstructive_pulmonary_disease dbr:Parkinson's_disease dbr:DNA_damage_(naturally_occurring) dbr:Mutation dbr:Helicase dbr:Nuclear_envelope dbr:Nuclear_localization_sequence dbr:Scaffold_protein dbr:Jack_(1996_film) dbr:Motivational_speaker dbr:Bloom_syndrome dbr:Base_excision_repair dbr:Malleolus dbr:Wrinkle dbr:Scarlett_Thomas dbr:Achilles_tendon dbr:Mutagen dbr:Fontanelle dbr:Fanconi_anemia dbr:Telangiectasia dbr:Lipoatrophy dbr:Wiedemann–Rautenstrauch_syndrome dbr:P53 dbr:Cornea dbr:Alopecia dbr:Arteriosclerosis dbr:Atherosclerosis dbr:Hypotrichosis dbr:Bleak_House dbr:Bloom_syndrome_protein dbr:Chromosomal_translocation dbr:Cockayne_syndrome dbr:The_Curious_Case_of_Benjamin_Button_(short_story) dbr:Epidermolytic_hyperkeratosis dbr:DDB2 dbr:ERCC4 dbr:ERCC5 dbr:ERCC6 dbr:RNA_polymerase_II dbr:Hayley_Okines dbr:Learning_disability dbr:Autosomal_dominant dbr:LMNA dbr:Scandinavia dbr:Puberty dbr:Meningioma dbr:Paa_(film) dbr:Hypogonadism dbr:Lipodystrophy dbr:Lesion dbr:Signal_transduction dbr:Ulcer dbr:DNA_mismatch_repair dbr:Lizzie_Velásquez dbr:Conserved_sequence dbr:Monogenic_(genetics) dbr:Midnight_Sun_(2006_film) dbr:Missense_mutation dbr:RecQ_helicase dbr:Homologous_recombination dbr:Restrictive_dermopathy dbr:TV_2_(Denmark) dbr:Werner_syndrome_ATP-dependent_helicase dbr:GTF2H5 dbr:MPLKIP dbr:Ocular dbr:ERCC8_(gene) dbr:Genetic_mutations dbr:Adolescent dbr:DNA_polymerase_eta dbr:RECQL dbr:XPA dbr:XPC_(gene) dbr:Sister_chromatid_exchange dbr:Farnesol dbr:Proteasome dbr:Transcription_factor_II_H dbr:Micrognathia dbr:Chaos;Child dbr:Eye_cancer dbr:Autosomal_recessive dbr:Dental_caries dbr:Cutaneous dbr:Transcription_(genetics) dbr:Pigmentary_retinopathy dbr:Neurodegeneration dbr:Cataracts dbr:File:Xeroderma_pigmentosum_02.jpg dbr:Noncoding_DNA dbr:Animal_models dbr:Marfan-progeroid-lipodystrophy_syndrome dbr:Metalloprotease dbr:Neonatal_progeroid_syndrome dbr:FBN1_(gene) dbr:IBIDS_syndrome dbr:Intercalating_agent dbr:Blood_vessels dbr:Membrane_receptors dbr:Protein_farnesyltransferase dbr:File:A_range_of_putative_disease-causing_mechanisms_for_the_case_of_HGPS.jpg dbr:File:Hutchinson-Gilford_Progeria_Syndrome.png dbr:Wikt:autochthonic dbr:File:Autosomal_recessive_-_en.svg
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dct:subject	dbc:Genetic_syndromes dbc:Aging-associated_diseases dbc:Progeroid_syndromes dbc:Senescence dbc:Rare_syndromes
gold:hypernym	dbr:Group
rdfs:label	Progeroid syndromes (en) متلازمات شبيهة الشياخ (ar) 早老症 (ja) 조로증 (ko)
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foaf:depiction	wiki-commons:Special:FilePath/Hutchinson-Gilford_Progeria_Syndrome.png wiki-commons:Special:FilePath/A_range_of_putative_d...g_mechanisms_for_the_case_of_HGPS.jpg wiki-commons:Special:FilePath/Autosomal_recessive_-_en.svg wiki-commons:Special:FilePath/Xeroderma_pigmentosum_02.jpg
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is dbo:wikiPageDisambiguates of	dbr:PS
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is dbo:wikiPageWikiLink of	dbr:List_of_syndromes dbr:ZMPSTE24 dbr:Lonafarnib dbr:DNA_repair-deficiency_disorder dbr:GAPO_syndrome dbr:DNA_damage_theory_of_aging dbr:PS dbr:Progeria dbr:Human_variability dbr:Sirtuin dbr:Familial_Amyloidosis,_Finnish_Type dbr:Early_aging dbr:Euchromatin dbr:DNA-(apurinic_or_apyrimidinic_site)_lyase dbr:Cellular_senescence dbr:Ataxia_telangiectasia_and_Rad3_related dbr:Georgette_Klinger dbr:Accelerated_aging_disease dbr:Mother's_Milk_(character) dbr:Premature_aging dbr:Asprosin dbr:SPRTN dbr:Aldehyde_dehydrogenase_18_family,_member_A1 dbr:POLD1 dbr:PYCR1 dbr:Sirtuin_7 dbr:Bruno_Reversade dbr:Genetics_of_aging dbr:Laura_Niedernhofer dbr:MDP_syndrome dbr:Jan_Karlseder dbr:Premature_aging_disease dbr:Premature_aging_syndrome dbr:Rapid_aging dbr:Progeroid_syndrome
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