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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 IDHuman Disease
147920 Kabuki Syndrome 1; KABUK1
300867 Kabuki Syndrome 2; KABUK2
612713 Kahrizi Syndrome; KHRZ
608207 Kala-Azar, Susceptibility to, 1; KAZA1
611381 Kala-Azar, Susceptibility to, 2; KAZA2
611382 Kala-Azar, Susceptibility to, 3; KAZA3
615953 Kallikrein, Decreased Urinary Activity of
308750 Kallmann Syndrome with Spastic Paraplegia
609242 Kanzaki Disease
148000 Kaposi Sarcoma, Susceptibility to (2 mouse models)
244300 Kapur-Toriello Syndrome
244450 Kaufman Oculocerebrofacial Syndrome (1 mouse models)
611775 Kawasaki Disease
148050 Kbg Syndrome; KBGS
530000 Kearns-Sayre Syndrome; KSS (2 mouse models)
300323 Kelley-Seegmiller Syndrome
148100 Keloid Formation
244460 Kenny-Caffey Syndrome, Type 1; KCS1
127000 Kenny-Caffey Syndrome, Type 2; KCS2
614098 Keppen-Lubinsky Syndrome; KPLBS
148200 Keratitis Fugax Hereditaria
148190 Keratitis, Hereditary (1 mouse models)
148210 Keratitis-Ichthyosis-Deafness Syndrome, Autosomal Dominant (1 mouse models)
148300 Keratoconus 1; KTCN1
608932 Keratoconus 2; KTCN2
608586 Keratoconus 3; KTCN3
609271 Keratoconus 4; KTCN4
614622 Keratoconus 5; KTCN5
614623 Keratoconus 6; KTCN6
614629 Keratoconus 7; KTCN7
614628 Keratoconus 8; KTCN8
244510 Keratoconus and Congenital Hip Dysplasia
244600 Keratoconus Posticus Circumscriptus; KPC
148350 Keratoderma, Palmoplantar, with Deafness
148360 Keratoderma, Palmoplantar, with Nail Dystrophy and Hereditary Motor-Sensory Neuropathy
148370 Keratolytic Winter Erythema
148390 Keratosis, Familial Actinic
148730 Keratosis, Focal Palmoplantar and Gingival
308830 Keratosis Follicularis, Dwarfism, and Cerebral Atrophy
612843 Keratosis Follicularis Spinulosa Decalvans, Autosomal Dominant; KFSD
308800 Keratosis Follicularis Spinulosa Decalvans, X-Linked; KFSDX
601952 Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma
148520 Keratosis Palmaris Et Plantaris with Clinodactyly
607654 Keratosis Palmoplantaris Striata III; PPKS3
612908 Keratosis Palmoplantaris Striata II; PPKS2
604093 Keratosis Pilaris
182000 Keratosis, Seborrheic (1 mouse models)
245130 Ketoadipicaciduria
182270 Ketone Compounds, Ability to Smell
245150 Keutel Syndrome (1 mouse models)
245180 Kifafa Seizure Disorder
173650 Kindler Syndrome (1 mouse models)
148800 Kleeblattschaedel
610253 Kleefstra Syndrome (2 mouse models)
148840 Kleine-Levin Hibernation Syndrome
118100 Klippel-Feil Syndrome 1, Autosomal Dominant; KFS1
214300 Klippel-Feil Syndrome 2, Autosomal Recessive; KFS2
613702 Klippel-Feil Syndrome 3, Autosomal Dominant; KFS3
149000 Klippel-Trenaunay-Weber Syndrome
604824 Klotho; KL (2 mouse models)
156550 Kniest Dysplasia
245190 Kniest-Like Dysplasia, Lethal
245160 Kniest-Like Dysplasia with Pursed Lips and Ectopia Lentis
267750 Knobloch Syndrome 1; KNO1 (1 mouse models)
149100 Knuckle Pads
149200 Knuckle Pads, Leukonychia, and Sensorineural Deafness
226750 Kohlschutter-Tonz Syndrome; KTZS
610443 Koolen-De Vries Syndrome; KDVS
262650 Kowarski Syndrome
245200 Krabbe Disease (3 mouse models)
611722 Krabbe Disease, Atypical, Due to Saposin A Deficiency
606693 Kufor-Rakeb Syndrome; KRS
245300 Kuru, Susceptibility to
211350 Kyphomelic Dysplasia
610170 Kyphoscoliosis 1; KYPSC1
149500 Kyrle Disease

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last database update
10/08/2014
MGI 5.20
The Jackson Laboratory