K - Health Conditions - Genetics Home Reference - NIH

K - Health Conditions - Genetics Home Reference - NIH

Health Conditions

Explore the signs and symptoms, genetic cause, and inheritance pattern of various health conditions.

• Kabuki make-up syndrome, see Kabuki syndrome
• Kabuki makeup syndrome, see Kabuki syndrome
• Kabuki syndrome
• Kahler disease, see Multiple myeloma
• Kahler's disease, see Multiple myeloma
• Kahler-Bozzolo disease, see Multiple myeloma
• Kallman's syndrome, see Kallmann syndrome
• Kallmann syndrome
• KANSL1-related intellectual disability syndrome, see Koolen-de Vries syndrome
• Kanzaki disease, see Schindler disease
• Kast syndrome, see Maffucci syndrome
• Kaufman oculocerebrofacial syndrome
• Kaufman-McKusick syndrome, see McKusick-Kaufman syndrome
• Kawasaki disease
• Kawasaki syndrome, see Kawasaki disease
• KBG syndrome
• KC, see Keratoconus
• KCNK9 imprinting syndrome
• KD, see Spinal and bulbar muscular atrophy
• KD, see Kawasaki disease
• KDVS, see Koolen-de Vries syndrome
• Kearns-Sayre mitochondrial cytopathy, see Kearns-Sayre syndrome
• Kearns-Sayre syndrome
• Keller syndrome, see FG syndrome
• Kennedy disease, see Spinal and bulbar muscular atrophy
• Kennedy spinal and bulbar muscular atrophy, see Spinal and bulbar muscular atrophy
• Kennedy's disease, see Spinal and bulbar muscular atrophy
• kerasin histiocytosis, see Gaucher disease
• kerasin lipoidosis, see Gaucher disease
• kerasin thesaurismosis, see Gaucher disease
• keratitis, ichthyosis, and deafness, see Keratitis-ichthyosis-deafness syndrome
• Keratitis-ichthyosis-deafness syndrome
• keratoconjunctivitis sicca, see Sjögren syndrome
• keratoconjunctivitis sicca-xerostomia, see Sjögren syndrome
• Keratoconus
• keratoderma hereditarium mutilans, see Vohwinkel syndrome
• Keratoderma with woolly hair
• Keratosis Follicularis, see Darier disease
• keratosis palmoplantaris transgrediens of Siemens, see Mal de Meleda
• ketoacidemia, see Maple syrup urine disease
• ketoacidosis due to SCOT deficiency, see Succinyl-CoA:3-ketoacid CoA transferase deficiency
• ketotic glycinemia, see Propionic acidemia
• ketotic hyperglycinemia, see Propionic acidemia
• KFS, see Klippel-Feil syndrome
• KHM, see Vohwinkel syndrome
• KID syndrome, see Keratitis-ichthyosis-deafness syndrome
• kidney Wilms tumor, see Wilms tumor
• kidney, adenomyosarcoma, embryonal, see Wilms tumor
• kidney, carcinosarcoma, embryonal, see Wilms tumor
• kidney, embryoma, see Wilms tumor
• kidney, embryonal mixed tumor, see Wilms tumor
• Kindler syndrome
• Kindler's syndrome, see Kindler syndrome
• Kinky Hair Syndrome, see Menkes syndrome
• Kjellin syndrome, see Spastic paraplegia type 15
• Kjer type optic atrophy, see Optic atrophy type 1
• Kjer's optic atrophy, see Optic atrophy type 1
• Kleefstra syndrome
• Klinefelter syndrome
• Klinefelter syndrome (KS), see Klinefelter syndrome
• Klinefelter's syndrome, see Klinefelter syndrome
• Klippel-Feil deformity, see Klippel-Feil syndrome
• Klippel-Feil sequence, see Klippel-Feil syndrome
• Klippel-Feil syndrome
• Klippel-Trenaunay disease, see Klippel-Trenaunay syndrome
• Klippel-Trenaunay syndrome
• KMS, see Kabuki syndrome
• Kniest chondrodystrophy, see Kniest dysplasia
• Kniest dysplasia
• Kniest syndrome, see Kniest dysplasia
• Knobloch syndrome
• knuckle pads, deafness, and leukonychia syndrome, see Bart-Pumphrey syndrome
• knuckle pads, leukonychia, and sensorineural deafness, see Bart-Pumphrey syndrome
• Kobberling-Dunnigan syndrome, see Familial partial lipodystrophy
• Koolen syndrome, see Koolen-de Vries syndrome
• Koolen-de Vries syndrome
• KOS, see Kaufman oculocerebrofacial syndrome
• Kostmann disease, see Severe congenital neutropenia
• Kostmann's agranulocytosis, see Severe congenital neutropenia
• Kostmann's syndrome, see Severe congenital neutropenia
• Krabbe disease
• Krause-Kivlin syndrome, see Peters plus syndrome
• Krause-van Schooneveld-Kivlin syndrome, see Peters plus syndrome
• KSS, see Kearns-Sayre syndrome
• KTS, see Klippel-Trenaunay syndrome
• Kugelberg-Welander syndrome, autosomal dominant, see Spinal muscular atrophy with lower extremity predominance
• Kuskokwim disease, see Kuskokwim syndrome
• Kuskokwim syndrome
• KWWH, see Keratoderma with woolly hair
• Kymenlaakso syndrome, see Lattice corneal dystrophy type II
• Published: December 4, 2018
• The resources on this site should not be used as a substitute for professional medical care or advice. Users with questions about a personal health condition should consult with a qualified healthcare professional.