{"id":269876,"date":"2024-06-26T09:31:26","date_gmt":"2024-06-26T07:31:26","guid":{"rendered":"https:\/\/staging.laboklin.com\/labogen\/labogen_wp\/index.php\/maladies-hereditaires-chat\/"},"modified":"2024-09-20T17:41:51","modified_gmt":"2024-09-20T15:41:51","slug":"maladies-hereditaires-chat","status":"publish","type":"page","link":"https:\/\/labogen.com\/fr\/maladies-hereditaires-chat\/","title":{"rendered":"Maladies h\u00e9r\u00e9ditaires – Chat"},"content":{"rendered":"\t\t
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Maladies h\u00e9r\u00e9ditaires – Chat<\/h3>
  • Acrodermatitis enteropathica (AE)<\/a><\/li>
  • Alpha-Mannosidosis (AMD)<\/a><\/li>
  • Atherosclerosis (ATH)<\/a><\/li>
  • Autoimmune lymphoproliferative syndrome (ALPS)<\/a><\/li>
  • Clopidogrel response<\/a><\/li>
  • Coat variant Sphynx \/ Devon Rex<\/a><\/li>
  • Congenital hypothyroidism (CH)<\/a><\/li>
  • Congenital myasthenic syndrome (CMS)<\/a><\/li>
  • Cystinuria<\/a><\/li>
  • Epileptic encephalopathy (EE)<\/a><\/li>
  • Factor XI deficiency (F11)<\/a><\/li>
  • Factor XII deficiency (F12)<\/a><\/li>
  • Gangliosidosis (GM1)<\/a><\/li>
  • Gangliosidosis (GM2) – Burmese<\/a><\/li>
  • Gangliosidosis (GM2) – Korat<\/a><\/li>
  • Genetic blood group<\/a><\/li>
  • Glycogen storage disease type IV (GSD4)<\/a><\/li>
  • Head Defect<\/a><\/li>
  • Hypertrophic cardiomyopathy (HCM1)<\/a><\/li>
  • Hypertrophic cardiomyopathy (HCM3)<\/a><\/li>
  • Hypertrophic cardiomyopathy (HCM4)<\/a><\/li>
  • Hypokalaemia<\/a><\/li>
  • Hypotrichosis and short life expectancy<\/a><\/li>
  • Mucopolysaccharidosis type VI (MPS6)<\/a><\/li>
  • Mucopolysaccharidosis type VII (MPS7)<\/a><\/li>
  • Myotonia congenita<\/a><\/li>
  • Osteochondrodysplasia (OCD)<\/a><\/li>
  • Polycystic kidney disease (PKD)<\/a><\/li>
  • Polydactyly<\/a><\/li>
  • Primary congenital glaucoma (PCG)<\/a><\/li>
  • Progressive retinal atrophy (b-PRA)<\/a><\/li>
  • Progressive retinal atrophy (pd-PRA)<\/a><\/li>
  • Progressive retinal atrophy (rdAc-PRA)<\/a><\/li>
  • Progressive retinal atrophy (rdy-PRA)<\/a><\/li>
  • Pyruvate kinase deficiency (PK)<\/a><\/li>
  • Skeletal dysplasia (SD)<\/a><\/li>
  • Spinal muscular atrophy (SMA)<\/a><\/li><\/div><\/div>\n\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t","protected":false},"excerpt":{"rendered":"","protected":false},"author":5,"featured_media":0,"parent":0,"menu_order":14,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-269876","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/labogen.com\/fr\/wp-json\/wp\/v2\/pages\/269876","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/labogen.com\/fr\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/labogen.com\/fr\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/labogen.com\/fr\/wp-json\/wp\/v2\/users\/5"}],"replies":[{"embeddable":true,"href":"https:\/\/labogen.com\/fr\/wp-json\/wp\/v2\/comments?post=269876"}],"version-history":[{"count":3,"href":"https:\/\/labogen.com\/fr\/wp-json\/wp\/v2\/pages\/269876\/revisions"}],"predecessor-version":[{"id":269879,"href":"https:\/\/labogen.com\/fr\/wp-json\/wp\/v2\/pages\/269876\/revisions\/269879"}],"wp:attachment":[{"href":"https:\/\/labogen.com\/fr\/wp-json\/wp\/v2\/media?parent=269876"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}