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 Alpha-N-acetylgalactosaminidase deficiency
• 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
• KCNB1 encephalopathy
• KCNB1-related epilepsy, see KCNB1 encephalopathy
• KCNK9 imprinting syndrome
• KD, see Kawasaki disease
• KD, see Spinal and bulbar muscular atrophy
• 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 calculi, see Kidney stones
• Kidney stone, see Kidney stones
• Kidney stones
• 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 epidermolysis bullosa
• Kindler syndrome, see Kindler epidermolysis bullosa
• Kindler's syndrome, see Kindler epidermolysis bullosa
• 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 dysplasia, COL2A1-related, see 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