Health Conditions - Genetics Home Reference | K [Kabuki make-up syndrome, see Kabuki syndrome]

Health Conditions - Genetics Home Reference

Health Conditions

Explore the signs and symptoms, frequency, genetic cause, and inheritance pattern of various conditions, diseases, and syndromes.

• 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
• 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
• 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
• 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'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
• Kuskokwim disease, see Kuskokwim syndrome
• Kuskokwim syndrome
• KWWH, see keratoderma with woolly hair
• Kymenlaakso syndrome, see lattice corneal dystrophy type II