MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4 552Gene
8 700Phänotypen
3,968 Erkrankungen gefunden (Kr.) Zurücksetzen

KLHL9-related early-onset distal myopathy

ORPHA:399081Kr.
Autosomal dominant

KRT1-related diffuse nonepidermolytic keratoderma

ORPHA:530838Kr.
Autosomal dominant

Kaposi sarcoma

ORPHA:33276Kr.
Not applicable

Kaposiform hemangioendothelioma

ORPHA:2122Kr.
Not applicable

Kaposiform lymphangiomatosis

ORPHA:464329Kr.
Not applicable

Karyomegalic interstitial nephritis

ORPHA:401996Kr.
Autosomal recessive

Kawasaki disease

ORPHA:2331Kr.
Multigenic/multifactorial

Kearns-Sayre syndrome

ORPHA:480Kr.
Autosomal recessive, Mitochondrial inheritance, Not applicable

Kennedy disease

ORPHA:481Kr.
X-linked recessive

Keratitis fugax hereditaria

ORPHA:647815Kr.
Autosomal dominant

Keratocystic odontogenic tumor

ORPHA:447777Kr.
Not applicable

Keratoderma hereditarium mutilans

ORPHA:494Kr.
Autosomal dominant

Keratoderma hereditarium mutilans with ichthyosis

ORPHA:79395Kr.
Autosomal dominant

Keratolytic winter erythema

ORPHA:50943Kr.
Autosomal dominant

Keratosis follicularis spinulosa decalvans

ORPHA:2340Kr.
Autosomal dominant, Autosomal recessive, X-linked recessive

Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome

ORPHA:281201Kr.
Autosomal recessive

Keratosis palmaris et plantaris-clinodactyly syndrome

ORPHA:86919Kr.
Autosomal dominant

Kerion celsi

ORPHA:499Kr.
Not applicable

Ketamine-induced biliary dilatation

ORPHA:293807Kr.
Not applicable

Ketoacidosis due to monocarboxylate transporter-1 deficiency

ORPHA:438075Kr.
Autosomal dominant, Autosomal recessive

Kidney tubulopathy-dilated cardiomyopathy syndrome

ORPHA:73224Kr.
Autosomal dominant

Kienbock disease

ORPHA:97332Kr.

Kikuchi-Fujimoto disease

ORPHA:50918Kr.

Kimura disease

ORPHA:482Kr.
Unknown