List of rare diseases-K
From WikiMD's WELLNESSPEDIA
NIH genetic and rare disease info[edit]
List of rare diseases-K is a rare disease.
| Rare and genetic diseases | ||||||
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Rare diseases - List of rare diseases-K
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- Kabuki make up syndrome
- Kabuki syndrome
- Kaeser syndrome
- Kagami-Ogata syndrome
- Kahler disease
- KAL1
- KAL2
- KAL3
- KAL4
- KAL5
- KAL6
- Kala-azar
- Kaler Garrity Stern syndrome
- Kallikrein attenuated hypertension
- Kallikrein hypertension
- Kallmann syndrome
- Kallmann syndrome 1
- Kallmann syndrome 2
- Kallmann syndrome 3
- Kallmann syndrome 4
- Kallmann syndrome 5
- Kallmann syndrome 6
- Kallmann syndrome, type 1, X-linked
- Kallmann syndrome, X-linked
- Kallmann's syndrome
- KANSL1-Related Intellectual Disability Syndrome
- Kantaputra mesomelic dysplasia
- Kanzaki disease
- Kaolin pneumoconiosis
- Kaplan Plauchu Fitch syndrome
- Kaposi sarcoma
- Kaposi sarcoma herpesvirus
- Kaposiform hemangio-endothelioma
- Kaposiform Hemangioendothelioma
- Kaposiform lymphangiomatosis
- Kaposi's sarcoma
- Kapur Toriello syndrome
- Karak syndrome
- KARAK SYNDROME, INCLUDED
- Karandikar Maria Kamble syndrome
- Karl Adolph von Basedow
- Karsch-Neugebauer syndrome
- Kartagener syndrome
- Karyomegalic interstitial nephritis
- Kasabach Merritt phenomenon
- Kasabach Merritt syndrome
- Kashani Strom Utley syndrome
- Kast Syndrome
- Kasznica Carlson Coppedge syndrome
- Katayama fever
- Katsantoni Papadakou Lagoyanni syndrome
- Kaufman McKusick syndrome
- Kaufman oculocerebrofacial syndrome
- Kawasaki disease
- Kawasaki syndrome
- Kawashima tsuji syndrome
- KBG syndrome
- KC
- KCNK9 imprinting syndrome
- KCNQ2-Related Disorders
- KCS1
- KCS2
- Kearns-Sayre syndrome
- kEDS
- kEDS-PLOD1
- Keipert Syndrome
- Keller syndrome
- Kelly-Paterson syndrome
- Kelly's syndrome
- Kennedy disease
- Kennerknecht Sorgo Oberhoffer syndrome
- Kenny-Caffey syndrome type 1
- Kenny-Caffey syndrome type 2
- Kenny-Caffey syndrome, autosomal dominant
- Kenny-Caffey syndrome, autosomal recessive
- Kerasin lipoidosis
- Kerasin thesaurismosis
- Keratitis sicca- not a rare disease.
- Keratitis, hereditary
- Keratitis, Ichthyosis, and Deafness (KID) Syndrome
- Keratitis-ichthyosis-deafness syndrome, autosomal dominant
- Keratitis-ichthyosis-deafness syndrome, autosomal recessive
- Keratitis-ichthyosis-deafness/Hystrix-like ichthyosis-deafness syndrome
- Keratoacanthoma
- Keratoactinomycosis
- Keratoconjunctivitis sicca- not a rare disease.
- Keratoconus
- Keratoconus posticus circumscriptus
- Keratoderma hereditarium mutilans
- Keratoderma palmoplantar deafness
- Keratoderma palmoplantar spastic paralysis
- Keratoderma palmoplantar striate form 3
- Keratoderma palmoplantar, punctate type 2
- Keratoderma palmoplantar, with deafness
- Keratoderma palmoplantaris transgrediens
- Keratoderma with woolly hair type II
- Keratoderma, hypotrichosis and leukonychia totalis
- Keratoderma, Palmoplantar
- Keratoderma, palmoplantar punctate type 1
- Keratoderma, palmoplantar striate form 1
- Keratoderma, palmoplantar, with nail dystrophy and hereditary motor-sensory neuropathy
- Keratodermia palmoplantar periorificial
- Keratodermia palmoplantaris papulosa, Buschke-Fischer-Brauer type
- Keratolysis exfoliativa congenita
- Keratolytic winter erythema
- Keratomalacia
- Keratoneuralgia
- Keratoris palmoplantaris with periodontopathia
- Keratosis exfoliativa congenita
- Keratosis extremitatum hereditaria progrediens
- Keratosis focal palmoplantar gingival
- Keratosis follicularis
- Keratosis follicularis dwarfism and cerebral atrophy
- Keratosis follicularis spinulosa decalvans
- Keratosis follicularis spinulosa decalvans cum ophiasi
- Keratosis of Greither
- Keratosis palmaris et plantaris with esophageal cancer
- Keratosis palmoplantar - periodontopathy
- Keratosis palmoplantaris arrythmogenic cardiomyopathy woolly hair
- Keratosis palmoplantaris papulosa
- Keratosis palmoplantaris striata 1
- Keratosis palmoplantaris striata 3
- Keratosis palmoplantaris transgradiens of Siemens
- Keratosis palmoplantaris transgrediens et progrediens
- Keratosis palmoplantaris with corneal dystrophy
- Keratosis palmoplantaris with esophageal cancer
- Keratosis palmoplantaris with periodontopathia
- Keratosis palmoplantaris with periodontopathia and onychogryposis
- Keratosis palmoplantaris-esophageal carcinoma syndrome
- Keratosis palmoplantar-periodontopathy syndrome
- Keratosis pilaris affecting the follicles of the eyebrow hairs
- Keratosis Seborrheica- not a rare disease.
- Keratosis, seborrheic- not a rare disease.
- Kerion celsi
- Kernicterus
- Kernicterus spectrum disorder
- Keshan disease
- Keto acid decarboxylase deficiency
- Ketoacidosis due to SCOT deficiency
- Ketoaciduria - intellectual disability - ataxia - deafness
- Ketoaciduria-intellectual disability-ataxia-deafness syndrome
- Ketoaciduria-mental deficiency syndrome
- Ketohexokinase deficiency- not a rare disease.
- Ketotic glycinemia
- Ketotic hyperglycinemia
- Keutel syndrome
- KFD
- KFD virus
- KFSD
- KH
- KHE
- KHM
- KICS
- KID syndrome
- KID syndrome, autosomal dominant
- KID syndrome, autosomal recessive
- KID/HID syndrome
- Kidney Medullary Carcinoma
- Kienbock disease
- Kienbock's disease
- Kifafa seizure disorder
- Kikuchi disease
- Kikuchi necrotizing lymphadenitis
- Kikuchi-Fujimoto disease
- Kikuchi-Fujimoto's disease
- Kikuchi's disease
- Killian syndrome
- Killian Teschler-Nicola syndrome
- Kimura disease
- KIN
- Kindler syndrome
- King Denborough syndrome
- King syndrome
- Kingella infections
- Kinky hair disease
- Kinky hair, photosensitivity, broken eyebrows and eyelashes, and nonprogressive mental retardation (formerly)
- Kinky or curly hair, dolichocephaly, enamel hypoplasia, increased dental caries, radial dense bones, and brittle nails
- Kinsbourne syndrome
- Kirghizian Dermatoosteolysis
- Kirner deformity
- Kitamura reticulate acropigmentation
- Kjellin syndrome
- Kjer-type optic atrophy
- Klatskin tumor
- Klatskin's tumor
- Klebsiella
- Klebsiella infection
- Kleeblattschaedel deformity syndrome
- Kleeblattschaedel syndrome
- Kleefstra syndrome
- Kleine Levin syndrome
- Kleine-Levin hibernation syndrome
- Kleiner Holmes syndrome
- Klein-Waardenburg syndrome
- Klinefelter syndrome- not a rare disease.
- Klinefelter's syndrome- not a rare disease.
- Klippel Feil syndrome
- Klippel Trenaunay syndrome
- Klippel-feil deformity, conductive deafness, and absent vagina
- Klippel-Feil syndrome with laryngeal malformation
- Klippel-Trenaunay syndrome
- Klippel-Trenaunay-Weber syndrome
- Klippel-Trénaunay-Weber syndrome
- Klumpke paralysis
- Klumpke's palsy
- Kluver Bucy syndrome
- KMP
- KMS
- KMT2B-Related Dystonia
- Knee replacement infection
- Kniest dysplasia
- Kniest like dysplasia lethal
- Kniest-like dysplasia with pursed lips and ectopia lentis
- Knobloch syndrome
- Knobloch-Layer syndrome
- KNS
- Knuckle pads, leuconychia and sensorineural deafness
- Knuckle pads-leukonychia-sensorineural deafness-palmoplantar hyperkeratosis syndrome
- Knuckle pads-leukonychia-sensorineural deafness-palmoplantar keratoderma syndrome
- Kocher Debre Semelaigne disease
- Kocher-Debre-Semelaigne syndrome
- Kochs disease
- Kohler disease
- Kohler's Disease
- Kohler's Disease of the Tarsal Navicular
- Kohler's Osteochondrosis of the Tarsal Navicular
- Kohler's second disease
- Kohlmeier-Degos disease
- Köhlmeier-Degos disease
- Köhlmeier-Degos-Delort-Tricort syndrome
- Kohlschutter syndrome
- Kohlschutter Tonz syndrome
- Kok disease
- Komuragaeri Disease
- Kônig disease
- König disease
- Koolen de Vries syndrome
- Koone Rizzo Elias syndrome
- Koro
- Koro syndrome
- KOS
- Kossard disease
- Kostmann disease
- Kosztolanyi syndrome
- Kotzot-Richter syndrome
- Kousseff Nichols syndrome
- Kousseff syndrome
- Kowarski syndrome
- Kozlowski Brown Hardwick syndrome
- Kozlowski Ouvrier syndrome
- Kozlowski Rafinski Klicharska syndrome
- Kozlowski Warren Fisher syndrome
- Kozlowski-Krajewska syndrome
- KPC
- Krabbe disease
- Krabbe disease atypical due to Saposin A deficiency
- Krabbe leukodystrophy
- Kraepelin disease
- Kramer syndrome
- KRAS gene related Noonan syndrome
- Krasnow Qazi syndrome
- Krasnow Qazi Yermakov syndrome
- Krause-Kivlin syndrome
- Krauss Herman Holmes syndrome
- Krieble Bixler syndrome
- KRPPD
- Krukenberg carcinoma
- Krukenberg tumor
- Krukenberg’s tumor
- KSHV
- KSHV inflammatory cytokine syndrome
- KSS
- KTS
- KTW syndrome
- Kufor-Rakeb syndrome
- Kufs disease
- Kuf's disease
- Kuf's disease type B
- Kuf's disease, autosomal dominant
- Kugelberg-Welander syndrome
- Kurczynski-Casperson syndrome
- Kuru
- Kuskokwim disease
- Kuskokwim syndrome
- Kuster syndrome
- Kuzniecky Andermann syndrome
- Kuzniecky syndrome
- KWE
- KWS
- KWWH type II
- Kyasanur Forest disease
- Kynureninase deficiency
- Kyphomelic dysplasia
- Kyphoscoliotic EDS
- Kyphoscoliotic EDS due to lysyl hydroxylase 1 deficiency
- Kyphoscoliotic Ehlers-Danlos syndrome
- Kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency
- Kyphosis brachyphalangy optic atrophy
- Kyrle disease
- Kyrle's disease
NIH genetic and rare disease info[edit]
List of rare diseases-K is a rare disease.
| Rare and genetic diseases | ||||||
|---|---|---|---|---|---|---|
|
Rare diseases - List of rare diseases-K
|
