{"id":270087,"date":"2024-06-26T09:32:13","date_gmt":"2024-06-26T07:32:13","guid":{"rendered":"https:\/\/staging.laboklin.com\/labogen\/labogen_wp\/index.php\/maladies-hereditaires-cheval\/"},"modified":"2024-09-26T16:21:52","modified_gmt":"2024-09-26T14:21:52","slug":"maladies-hereditaires-cheval","status":"publish","type":"page","link":"https:\/\/labogen.com\/fr\/maladies-hereditaires-cheval\/","title":{"rendered":"Maladies h\u00e9r\u00e9ditaires – cheval"},"content":{"rendered":"\t\t
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Maladies h\u00e9r\u00e9ditaires – cheval<\/h3>
  • Androgen insensitivity syndrome (AR1)<\/a><\/li>
  • Androgen insensitivity syndrome (AR2, AR3, AR4, AR5)*<\/a><\/li>
  • Cerebellar abiotrophy (CA)<\/a><\/li>
  • Congenital stationary night blindness (CSNB2)*<\/a><\/li>
  • Distichiasis<\/a><\/li>
  • Dwarfism<\/a><\/li>
  • Dwarfism (ACAN, Chrondrodysplasie)<\/a><\/li>
  • Equine juvenile spinozerebell\u00e4re ataxia (EJSCA)<\/a><\/li>
  • Equine malignant hyperthermia (EMH)<\/a><\/li>
  • Foal immunodeficiency syndrome (FIS)<\/a><\/li>
  • Glycogen branching enzyme deficiency (GBED)<\/a><\/li>
  • Hereditary eqine regional dermal asthenia (HERDA)<\/a><\/li>
  • Hereditary junctional epidermolysis bullosa (JEB1)<\/a><\/li>
  • Hereditary myotonia (NFP)<\/a><\/li>
  • Hoof wall separation disease (HWSD)<\/a><\/li>
  • Hydrocephalus<\/a><\/li>
  • Hyperkalemic periodic paralysis (HYPP)<\/a><\/li>
  • Hypertriglyceridemia-induced pancreatitis (HIP)<\/a><\/li>
  • Idiopathic hypocalcemia<\/a><\/li>
  • Immune Mediated Myositis & MYH1 Myopathy (MYHM)<\/a><\/li>
  • Junctional epidermolysis bullosa (JEB2)*<\/a><\/li>
  • Lavender foal syndrome (LFS)<\/a><\/li>
  • Lethal white foal syndrome (LWO)<\/a><\/li>
  • Naked Foal Syndrome (NFS)<\/a><\/li>
  • Occipitoatlantoaxial Malformation (OAAM)<\/a><\/li>
  • Ocular Squamous Cell Carcinoma (SCC)<\/a><\/li>
  • Polysaccharid storage myopathy type 1 (PSSM)<\/a><\/li>
  • Predictive height test<\/a><\/li>
  • Severe combined immunodeficiency (SCID)<\/a><\/li>
  • Skeletal atavism (SA)<\/a><\/li>
  • Speed gene<\/a><\/li>
  • SynchroGait (DMRT3)<\/a><\/li>
  • Tiger eye*<\/a><\/li>
  • Tractability<\/a><\/li>
  • Warmblood fragile foal syndrome (WFFS)<\/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":15,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-270087","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/labogen.com\/fr\/wp-json\/wp\/v2\/pages\/270087","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=270087"}],"version-history":[{"count":1,"href":"https:\/\/labogen.com\/fr\/wp-json\/wp\/v2\/pages\/270087\/revisions"}],"predecessor-version":[{"id":270088,"href":"https:\/\/labogen.com\/fr\/wp-json\/wp\/v2\/pages\/270087\/revisions\/270088"}],"wp:attachment":[{"href":"https:\/\/labogen.com\/fr\/wp-json\/wp\/v2\/media?parent=270087"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}