MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4,552Gene
8,700Phänotypen

Lymphangioleiomyomatosis

ORPHA:538Kr.
Not applicable

Lymphatic filariasis

ORPHA:2035Kr.
Not applicable

Lymphedema with yellow nails

ORPHA:662Kr.

Lymphedema-atrial septal defects-facial changes syndrome

ORPHA:86915Malf.
Autosomal recessive

Lymphedema-cerebral arteriovenous anomaly-primary pulmonary hypertension syndrome

ORPHA:86914Malf.

Lymphedema-distichiasis syndrome

ORPHA:33001Malf.
Autosomal dominant

Lymphedema-posterior choanal atresia syndrome

ORPHA:99141Malf.
Autosomal recessive

Lymphocytic hypereosinophilic syndrome

ORPHA:314970Kl. subt.

Lymphoid interstitial pneumonia

ORPHA:79128Kr.
Not applicable

Lymphomatoid granulomatosis

ORPHA:86869Kr.
Not applicable

Lymphomatoid papulosis

ORPHA:98842Kr.

Lymphoplasmacytic inflammatory pseudotumor of the liver

ORPHA:555437Kl. subt.

Lymphoplasmacytic lymphoma without IgM production

ORPHA:443159Kr.
Not applicable

Lymphoproliferative disease associated with primary immune disease

ORPHA:98291Kat.

Lynch syndrome

ORPHA:144Kr.
Autosomal dominant

Lysinuric protein intolerance

ORPHA:470Kr.
Autosomal recessive

Lysosomal acid lipase deficiency

ORPHA:275761Kr.
Autosomal recessive

Lysosomal acid phosphatase deficiency

ORPHA:35121Kr.
Autosomal recessive

Léri-Weill dyschondrosteosis

ORPHA:240Malf.
Autosomal dominant

MADD-related developmental delay-endocrine dysfunction-hypohemoglobinemia syndrome

ORPHA:686495Kr.
Autosomal recessive

MAGIC syndrome

ORPHA:324972Kr.

MALT lymphoma

ORPHA:52417Kr.
Multigenic/multifactorial, Not applicable

MAN1B1-CDG

ORPHA:397941Kr.
Autosomal recessive

MAN2B2-CDG

ORPHA:695110Kr.
Autosomal recessive