Human Disease Vocabulary Browser

The current vocabulary contains human disease, syndrome, and condition terms from Online Mendelian Inheritance in Man (OMIM database).

Browse vocabulary terms by beginning character

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Human Diseases/Syndromes Beginning with "K"

To see all annotations for a disease, click the disease name.

OMIM ID	Human Disease
OMIM:147920	Kabuki Syndrome 1; KABUK1
OMIM:300867	Kabuki Syndrome 2; KABUK2
OMIM:608149	Kagami-Ogata Syndrome
OMIM:612713	Kahrizi Syndrome; KHRZ
OMIM:608207	Kala-Azar, Susceptibility to, 1; KAZA1
OMIM:611381	Kala-Azar, Susceptibility to, 2; KAZA2
OMIM:611382	Kala-Azar, Susceptibility to, 3; KAZA3
OMIM:615953	Kallikrein, Decreased Urinary Activity of
OMIM:308750	Kallmann Syndrome with Spastic Paraplegia
OMIM:609242	Kanzaki Disease
OMIM:148000	Kaposi Sarcoma, Susceptibility to
OMIM:244300	Kapur-Toriello Syndrome
OMIM:620985	Karayol-Borroto-Haghshenas Neurodevelopmental Syndrome; KBHS
OMIM:620937	Kariminejad-Reversade Neurodevelopmental Syndrome; KAREVS
OMIM:244450	Kaufman Oculocerebrofacial Syndrome; KOS
OMIM:611775	Kawasaki Disease
OMIM:619125	Kaya-Barakat-Masson Syndrome; KABAMAS
OMIM:148050	Kbg Syndrome; KBGS
OMIM:530000	Kearns-Sayre Syndrome; KSS
OMIM:301026	Keipert Syndrome; KPTS
OMIM:148100	Keloid Formation; KLDF
OMIM:244460	Kenny-Caffey Syndrome, Type 1; KCS1
OMIM:127000	Kenny-Caffey Syndrome, Type 2; KCS2
OMIM:614098	Keppen-Lubinsky Syndrome; KPLBS
OMIM:148190	Keratitis, Hereditary
OMIM:148210	Keratitis-Ichthyosis-Deafness Syndrome, Autosomal Dominant; KIDAD
OMIM:242150	Keratitis-Ichthyosis-Deafness Syndrome, Autosomal Recessive; KIDAR
OMIM:148300	Keratoconus 1; KTCN1
OMIM:608932	Keratoconus 2; KTCN2
OMIM:608586	Keratoconus 3; KTCN3
OMIM:609271	Keratoconus 4; KTCN4
OMIM:614622	Keratoconus 5; KTCN5
OMIM:614623	Keratoconus 6; KTCN6
OMIM:614629	Keratoconus 7; KTCN7
OMIM:614628	Keratoconus 8; KTCN8
OMIM:617928	Keratoconus 9; KTCN9
OMIM:244510	Keratoconus and Congenital Hip Dysplasia
OMIM:244600	Keratoconus Posticus Circumscriptus; KPC
OMIM:620009	Keratoderma-Ichthyosis-Deafness Syndrome, Autosomal Recessive; KDIDAR
OMIM:148350	Keratoderma, Palmoplantar, with Deafness
OMIM:148360	Keratoderma, Palmoplantar, with Nail Dystrophy and Hereditary Motor-Sensory Neuropathy
OMIM:148200	Keratoendotheliitis Fugax Hereditaria; KEFH
OMIM:148370	Keratolytic Winter Erythema; KWE
OMIM:148390	Keratosis, Familial Actinic
OMIM:148730	Keratosis, Focal Palmoplantar and Gingival
OMIM:308830	Keratosis Follicularis, Dwarfism, and Cerebral Atrophy
OMIM:612843	Keratosis Follicularis Spinulosa Decalvans, Autosomal Dominant; KFSD
OMIM:308800	Keratosis Follicularis Spinulosa Decalvans, X-Linked; KFSDX
OMIM:601952	Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma; KLICK
OMIM:148520	Keratosis Palmaris Et Plantaris with Clinodactyly
OMIM:607654	Keratosis Palmoplantaris Striata III; PPKS3
OMIM:612908	Keratosis Palmoplantaris Striata II; PPKS2
OMIM:604093	Keratosis Pilaris Atrophicans; KPA
OMIM:182000	Keratosis, Seborrheic
OMIM:182270	Ketone Compounds, Ability to Smell
OMIM:245150	Keutel Syndrome; KTLS
OMIM:618460	Khan-Khan-Katsanis Syndrome; 3KS
OMIM:245180	Kifafa Seizure Disorder
OMIM:619080	Kilquist Syndrome; KILQS
OMIM:173650	Kindler Syndrome; KNDLRS
OMIM:619542	King-Denborough Syndrome; KDS
OMIM:619297	Kinsship Syndrome; KINS
OMIM:148800	Kleeblattschaedel
OMIM:610253	Kleefstra Syndrome 1; KLEFS1
OMIM:617768	Kleefstra Syndrome 2; KLEFS2
OMIM:148840	Kleine-Levin Hibernation Syndrome
OMIM:118100	Klippel-Feil Syndrome 1, Autosomal Dominant; KFS1
OMIM:214300	Klippel-Feil Syndrome 2, Autosomal Recessive; KFS2
OMIM:613702	Klippel-Feil Syndrome 3, Autosomal Dominant; KFS3
OMIM:616549	Klippel-Feil Syndrome 4, Autosomal Recessive, with Nemaline Myopathy and Facial Dysmorphism; KFS4
OMIM:149000	Klippel-Trenaunay-Weber Syndrome
OMIM:156550	Kniest Dysplasia
OMIM:245190	Kniest-Like Dysplasia, Lethal
OMIM:245160	Kniest-Like Dysplasia with Pursed Lips and Ectopia Lentis
OMIM:267750	Knobloch Syndrome 1; KNO1
OMIM:618458	Knobloch Syndrome 2; KNO2
OMIM:149100	Knuckle Pads
OMIM:226750	Kohlschutter-Tonz Syndrome; KTZS
OMIM:606242	Kondoh Syndrome
OMIM:610443	Koolen-De Vries Syndrome; KDVS
OMIM:616592	Kosaki Overgrowth Syndrome; KOGS
OMIM:262650	Kowarski Syndrome
OMIM:611722	Krabbe Disease, Atypical, Due to Saposin A Deficiency; KRBSAPA
OMIM:245200	Krabbe Disease; KRB
OMIM:606693	Kufor-Rakeb Syndrome; KRS
OMIM:245300	Kuru, Susceptibility to
OMIM:619762	Kury-Isidor Syndrome; KURIS
OMIM:211350	Kyphomelic Dysplasia
OMIM:610170	Kyphoscoliosis 1; KYPSC1
OMIM:149500	Kyrle Disease

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