Disease Name Symbol Acronym
Kabuki Syndrome 1 KBK002
Kabuki Syndrome 2 KBK003
Kagami-Ogata Syndrome KGM001
Kahrizi Syndrome KHR001
Kala-Azar 1 KLZ004
Kala-Azar 2 KLZ002
Kala-Azar 3 KLZ003
Kallmann Syndrome KLL001
Kallmann Syndrome 3 KLL005
Kallmann Syndrome 4 KLL006
Kallmann Syndrome 5 KLL007
Kallmann Syndrome 6 KLL008
Kanzaki Disease KNZ001
Kaolin Pneumoconiosis KLN003
Kaposi Sarcoma KPS004
Kaposiform Hemangioendothelioma KPS002
Kappa Light Chain Deficiency KPP001
Karak Syndrome KRK002
Kars-Related Intermediate Charcot-Marie-Tooth Neuropathy KRS002
Kartagener Syndrome KRT010
Kashin-Beck Disease KSH004
Kat6b-Related Disorders KT6001
Kaufman Oculocerebrofacial Syndrome KFM001
Kawasaki Disease KWS002
Kbg Syndrome KBG001
Kbtbd13-Related Nemaline Myopathy KBT001
Kcna5-Related Familial Atrial Fibrillation KCN001
Kcne2-Related Familial Atrial Fibrillation KCN002
Kcne5-Related Atrial Fibrillation KCN018
Kcnj10-Related Pendred Syndrome KCN003
Kcnj11-Related Hyperinsulinism KCN004
Kcnj11-Related Permanent Neonatal Diabetes Mellitus KCN005
Kcnj11-Related Susceptibility to Noninsulin-Dependent Diabetes Mellitus KCN006
Kcnj13-Related Leber Congenital Amaurosis KCN007
Kcnj2-Related Familial Atrial Fibrillation KCN008
Kcnq1-Related Familial Atrial Fibrillation KCN009
Kcnq2-Related Disorders KCN010
Kcnq3-Related Benign Familial Neonatal Epilepsy KCN011
Kcnq3-Related Disorders KCN014
Kcnt1 Epileptic Encephalopathy, Early Infantile, 14 KCN015
Kcnt1-Related Nocturnal Frontal Lobe Epilepsy, Autosomal Dominant KCN016
Kdm6a-Related Kabuki Syndrome KDM001
Kearns-Sayre Syndrome KRN002
Keloid Formation KLD003
Keloids KLD001
Kenny-Caffey Syndrome KNN002
Kenny-Caffey Syndrome, Type 1 KNN009
Kenny-Caffey Syndrome, Type 2 KNN007
Keppen-Lubinsky Syndrome KPP002
Keratinizing Squamous Cell Carcinoma KRT003
Keratitis KRT004
Keratitis-Ichthyosis-Deafness Syndrome KRT011
Keratoacanthoma KRT005
Keratoconjunctivitis KRT006
Keratoconus KRT007
Keratoconus 1 KRT029
Keratoconus 2 KRT039
Keratoconus 3 KRT040
Keratoconus 4 KRT041
Keratoconus 5 KRT050
Keratoconus 6 KRT052
Keratoconus 7 KRT053
Keratoconus 8 KRT054
Keratocystic Odontogenic Tumor KRT063
Keratoderma with Woolly Hair KRT062
Keratoderma, Palmoplantar, Punctate Type Ia KRT055
Keratoderma, Palmoplantar, with Deafness KRT058
Keratolytic Winter Erythema KRT013
Keratomalacia KRT002
Keratopathy KRT008
Keratosis KRT009
Keratosis Follicularis Spinulosa Decalvans KRT014
Keratosis Follicularis Spinulosa Decalvans, X-Linked KRT057
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma KRT038
Keratosis Palmoplantaris Striata KRT059
Keratosis Palmoplantaris Striata I, Ad KRT056
Keratosis Palmoplantaris Striata Ii KRT017
Keratosis Palmoplantaris Striata Iii KRT018
Keratosis Pilaris KRT044
Keratosis, Seborrheic, Somatic KRT036
Kernicterus KRN004
Keshan Disease KSH001
Ketothiolase Deficiency KTT001
Keutel Syndrome KTL001
Kiaa0586-Related Joubert Syndrome K05001
Kiaa2022-Related X-Linked Mental Retardation K20001
Kid Syndrome KDS001
Kidney Angiomyolipoma KDN015
Kidney Benign Neoplasm KDN016
Kidney Cancer KDN017
Kidney Clear Cell Sarcoma KDN007
Kidney Cortex Necrosis KDN001
Kidney Disease CHL091
Kidney Fibrosarcoma KDN009
Kidney Hemangiopericytoma KDN004
Kidney Hypertrophy KDN013
Kidney Leiomyosarcoma KDN014
Kidney Lipoma KDN003
Kidney Papillary Necrosis KDN006
Kidney Rhabdoid Cancer KDN002
Kidney Sarcoma KDN019
Kif14-Related Meckel Syndrome KF1003
Kif1b-Related Neuroblastoma, Susceptibility KF1001
Kif1b-Related Pheochromocytoma KF1002
Kif21a-Related Congenital Fibrosis of the Extraocular Muscles KF2001
Kif7-Related Joubert Syndrome KF7001
Kikuchi Disease KKC001
Kimura Disease KMR001
Kindler Syndrome KND001
Kiss1-Related Isolated Gonadotropin-Releasing Hormone Deficiency KSS003
Kiss1r-Related Isolated Gonadotropin-Releasing Hormone Deficiency KSS002
Klatskin's Tumor KLT001
Klebsiella Infection KLB004
Kleeblattschaedel Syndrome KLB002
Kleefstra Syndrome KLF001
Kleefstra Syndrome Due to 9q34 Microdeletion KLF003
Kleefstra Syndrome Due to a Point Mutation KLF002
Kleine-Levin Hibernation Syndrome KLN009
Kleptomania KLP001
Klhl40-Related Nemaline Myopathy KLH003
Klhl41-Related Nemaline Myopathy KLH004
Klhl7-Related Retinitis Pigmentosa KLH001
Klhl9-Related Childhood-Onset Distal Myopathy KLH002
Klinefelter's Syndrome KLN001
Klippel-Feil Syndrome KLP003
Klippel-Feil Syndrome 1 KLP012
Klippel-Feil Syndrome 1, Autosomal Dominant KLP007
Klippel-Feil Syndrome 2 KLP009
Klippel-Feil Syndrome 3 KLP013
Klippel-Feil Syndrome 3, Autosomal Dominant KLP006
Klippel-Feil Syndrome 4 KLP015
Klippel-Feil Syndrome 4, Autosomal Recessive, with Myopathy and Facial Dysmorphism KLP011
Klippel-Trenaunay-Weber Syndrome KLP010
Kluver-Bucy Syndrome KLV001
Kmt2d-Related Kabuki Syndrome KMT001
Kniest Dysplasia KNS001
Knobloch Syndrome KNB001
Knobloch Syndrome, Type 1 KNB004
Kohlschutter-Tonz Syndrome KHL003
Kondoh Syndrome KND003
Koolen-De Vries Syndrome KLN006
Koolen-De Vries Syndrome Due to a Point Mutation KLN007
Korean Hemorrhagic Fever KRN001
Koro KR001
Kosaki Overgrowth Syndrome KSK002
Kowarski Syndrome KWR001
Krabbe Disease KRB001
Krabbe Disease, Atypical KRB004
Kras-Related Cardiofaciocutaneous Syndrome KRS003
Kras-Related Noonan Syndrome KRS004
Krt1-Related Epidermolytic Hyperkeratosis KRT033
Krt10-Related Epidermolytic Hyperkeratosis KRT030
Krt16-Related Pachyonychia Congenita KRT031
Krt17-Related Pachyonychia Congenita KRT032
Krt6a-Related Pachyonychia Congenita KRT034
Krt6b-Related Pachyonychia Congenita KRT035
Krukenberg Carcinoma KRK001
Kufor-Rakeb Syndrome KFR001
Kummell's Disease KMM001
Kuru KR002
Kwashiorkor KWS001
Kyasanur Forest Disease KYS001
Kyphoscoliosis 1 KYP003