2018-05-29 release

New classes:

• vascular bone neoplasm
• glioma susceptibility 1
• familial chronic mucocutaneous candidiasis
• papillary urothelial hyperplasia
• tumor grading characteristic
• nail infection
• general tumor grading characteristic
• dermatosis of eyelid
• eccrine sweat gland hamartoma
• skin appendage disease
• urothelial hyperplasia
• spondyloarthropathy, susceptibility to
• familial acne inversa
• reactive thrombocytosis
• schwannomatosis 1
• renal hypodysplasia/aplasia 1
• appendix neuroendocrine neoplasm
• duodenal neuroendocrine neoplasm
• digestive system neuroendocrine neoplasm
• gallbladder neuroendocrine neoplasm
• disorder of anatomical region
• enterochromaffin cell serotonin-producing pancreatic neuroendocrine tumor
• aniridia 1
• Adams-Oliver syndrome 1
• epilepsy, hot water, 1
• bethlem myopathy 1
• otofaciocervical syndrome 1
• myopathy, tubular aggregate, 1
• Dowling-Degos disease 1
• pulmonary hypertension, primary, 1
• glucocorticoid deficiency 1
• Singleton-Merten syndrome 1
• basal ganglia calcification, idiopathic, 1
• Brown-Vialetto-van Laere syndrome 1
• choroidal dystrophy, central areolar, 1
• AAA1
• renal hypodysplasia/aplasia 3
• aortic valve disease 1
• amyloidosis, primary localized cutaneous, 1
• FRTS1
• DUH1
• GFND1
• Zimmermann-Laband syndrome 1
• MVP1
• progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 1
• linear skin defects with multiple congenital anomalies 1
• lymphoproliferative syndrome, X-linked, 1
• D-2-hydroxyglutaric aciduria 1
• myopathy, lactic acidosis, and sideroblastic anemia 1
• epilepsy, familial focal, with variable foci 1
• megalencephalic leukoencephalopathy with subcortical cysts 1
• radioulnar synostosis with amegakaryocytic thrombocytopenia 1
• ataxia-telangiectasia-like disorder 1
• frontometaphyseal dysplasia 1
• AAT1
• trichohepatoenteric syndrome 1
• Jervell and Lange-Nielsen syndrome 1
• brittle cornea syndrome 1
• cerebellar ataxia, mental retardation, and dysequilibrium syndrome 1
• Miyoshi muscular dystrophy 1
• Heimler syndrome 1
• pancreatic agenesis 1
• hypertrophic osteoarthropathy, primary, autosomal recessive, 1
• MCOPCB1
• peeling skin syndrome 1
• hyperparathyroidism 4
• herpes simplex encephalitis, susceptibility to, 1
• sick sinus syndrome 1
• ectodermal dysplasia-syndactyly syndrome 1
• cerebroretinal microangiopathy with calcifications and cysts 1
• hypotonia, infantile, with psychomotor retardation and characteristic facies 1
• febrile seizures, familial, 11
• OPA8
• infantile liver failure syndrome 1
• macular dystrophy, vitelliform, 3
• PDA1
• squamous cell intraepithelial neoplasia
• intraepithelial neoplasia
• liver and intrahepatic bile duct neoplasm
• epithelial neoplasm of rectum
• epithelial tumor of colon
• mesenchymal hamartoma
• Astrakhan spotted fever
• Boutonneuse fever
• tumor grade 3 or 4, general grading system
• tumor grade 2 or 3, general grading system
• tumor grade 1, general grading system
• tumor grade X, general grading system
• tumor grade 3, general grading system
• tumor grade 2, general grading system
• tumor grade 1 or 2, general grading system
• tumor grade 4, general grading system