MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов

Kawasaki disease

ORPHA:2331Заболевание
Multigenic/multifactorial

Kearns-Sayre syndrome

ORPHA:480Заболевание
Autosomal recessive, Mitochondrial inheritance, Not applicable

Keipert syndrome

ORPHA:2662Мальформация
X-linked recessive

Kennedy disease

ORPHA:481Заболевание
X-linked recessive

Kenny-Caffey syndrome

ORPHA:2333Мальформация
Autosomal dominant, Autosomal recessive

Keppen-Lubinsky syndrome

ORPHA:435628Мальформация
Autosomal dominant, Not applicable

Keratinopathic ichthyosis

ORPHA:281103Клин. группа

Keratitis fugax hereditaria

ORPHA:647815Заболевание
Autosomal dominant

Keratocystic odontogenic tumor

ORPHA:447777Заболевание
Not applicable

Keratoderma hereditarium mutilans

ORPHA:494Заболевание
Autosomal dominant

Keratoderma hereditarium mutilans with ichthyosis

ORPHA:79395Заболевание
Autosomal dominant

Keratolytic winter erythema

ORPHA:50943Заболевание
Autosomal dominant

Keratosis follicularis spinulosa decalvans

ORPHA:2340Заболевание
Autosomal dominant, Autosomal recessive, X-linked recessive

Keratosis follicularis-dwarfism-cerebral atrophy syndrome

ORPHA:2339Мальформация
X-linked recessive

Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome

ORPHA:281201Заболевание
Autosomal recessive

Keratosis palmaris et plantaris-clinodactyly syndrome

ORPHA:86919Заболевание
Autosomal dominant

Kerion celsi

ORPHA:499Заболевание
Not applicable

Ketamine-induced biliary dilatation

ORPHA:293807Заболевание
Not applicable

Ketoacidosis due to monocarboxylate transporter-1 deficiency

ORPHA:438075Заболевание
Autosomal dominant, Autosomal recessive

Keutel syndrome

ORPHA:85202Мальформация
Autosomal recessive

Kidney tubulopathy-dilated cardiomyopathy syndrome

ORPHA:73224Заболевание
Autosomal dominant

Kienbock disease

ORPHA:97332Заболевание

Kikuchi-Fujimoto disease

ORPHA:50918Заболевание

Kimura disease

ORPHA:482Заболевание
Unknown