Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
KLHL9-related early-onset distal myopathy
Autosomal dominant
Adolescent, Childhood
KRT1-related diffuse nonepidermolytic keratoderma
Autosomal dominant
Childhood, Infancy
Kaposi sarcoma
Not applicable
Adult
Kaposiform hemangioendothelioma
Not applicable
All ages
Kaposiform lymphangiomatosis
Not applicable
Childhood
Karyomegalic interstitial nephritis
Autosomal recessive
Adult
Kawasaki disease
Multigenic/multifactorial
Adolescent, Adult, Childhood, Infancy
Kearns-Sayre syndrome
Autosomal recessive, Mitochondrial inheritance, Not applicable
Adolescent, Adult, Childhood, Infancy
Kennedy disease
X-linked recessive
Adult
Keratitis fugax hereditaria
Autosomal dominant
Keratocystic odontogenic tumor
Not applicable
Keratoderma hereditarium mutilans
Autosomal dominant
Childhood, Infancy
Keratoderma hereditarium mutilans with ichthyosis
Autosomal dominant
Infancy, Neonatal
Keratolytic winter erythema
Autosomal dominant
Adolescent, Adult, Childhood, Infancy, Neonatal
Keratosis follicularis spinulosa decalvans
Autosomal dominant, Autosomal recessive, X-linked recessive
Childhood
Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome
Autosomal recessive
Infancy, Neonatal
Keratosis palmaris et plantaris-clinodactyly syndrome
Autosomal dominant
Neonatal
Kerion celsi
Not applicable
All ages
Ketamine-induced biliary dilatation
Not applicable
All ages
Ketoacidosis due to monocarboxylate transporter-1 deficiency
Autosomal dominant, Autosomal recessive
Childhood, Infancy
Kidney tubulopathy-dilated cardiomyopathy syndrome
Autosomal dominant
Childhood
Kienbock disease
Adult
Kikuchi-Fujimoto disease
Adolescent, Adult, Childhood, Infancy
Kimura disease
Unknown
Adult