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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).

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Human Diseases/Syndromes Beginning with "K"

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

OMIM IDHuman 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:244450 Kaufman Oculocerebrofacial Syndrome; KOS
OMIM:611775 Kawasaki Disease
OMIM:148050 Kbg Syndrome; KBGS
OMIM:530000 Kearns-Sayre Syndrome; KSS
OMIM:300323 Kelley-Seegmiller Syndrome
OMIM:148100 Keloid Formation
OMIM:600908 Kennerknecht Syndrome
OMIM:244460 Kenny-Caffey Syndrome, Type 1; KCS1
OMIM:127000 Kenny-Caffey Syndrome, Type 2; KCS2
OMIM:614098 Keppen-Lubinsky Syndrome; KPLBS
OMIM:148200 Keratitis Fugax Hereditaria
OMIM:148190 Keratitis, Hereditary
OMIM:148210 Keratitis-Ichthyosis-Deafness Syndrome, Autosomal Dominant
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:244510 Keratoconus and Congenital Hip Dysplasia
OMIM:244600 Keratoconus Posticus Circumscriptus; KPC
OMIM:148350 Keratoderma, Palmoplantar, with Deafness
OMIM:148360 Keratoderma, Palmoplantar, with Nail Dystrophy and Hereditary Motor-Sensory Neuropathy
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;
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:245130 Ketoadipicaciduria
OMIM:182270 Ketone Compounds, Ability to Smell
OMIM:245150 Keutel Syndrome; KTLS
OMIM:245180 Kifafa Seizure Disorder
OMIM:173650 Kindler Syndrome; KNDLRS
OMIM:148800 Kleeblattschaedel
OMIM:610253 Kleefstra Syndrome
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:604824 Klotho; KL
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:149100 Knuckle Pads
OMIM:149200 Knuckle Pads, Leukonychia, and Sensorineural Deafness
OMIM:226750 Kohlschutter-Tonz Syndrome; KTZS
OMIM:610443 Koolen-De Vries Syndrome; KDVS
OMIM:616592 Kosaki Overgrowth Syndrome; KOGS
OMIM:262650 Kowarski Syndrome
OMIM:245200 Krabbe Disease
OMIM:611722 Krabbe Disease, Atypical, Due to Saposin A Deficiency
OMIM:606693 Kufor-Rakeb Syndrome; KRS
OMIM:245300 Kuru, Susceptibility to
OMIM:211350 Kyphomelic Dysplasia
OMIM:610170 Kyphoscoliosis 1; KYPSC1
OMIM:149500 Kyrle Disease

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last database update
06/13/2017
MGI 6.10
The Jackson Laboratory