MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes

Lymphangioleiomyomatosis

ORPHA:538Disease
Not applicable

Lymphatic filariasis

ORPHA:2035Disease
Not applicable

Lymphedema with yellow nails

ORPHA:662Disease

Lymphedema-atrial septal defects-facial changes syndrome

ORPHA:86915Malform.
Autosomal recessive

Lymphedema-cerebral arteriovenous anomaly-primary pulmonary hypertension syndrome

ORPHA:86914Malform.

Lymphedema-distichiasis syndrome

ORPHA:33001Malform.
Autosomal dominant

Lymphedema-posterior choanal atresia syndrome

ORPHA:99141Malform.
Autosomal recessive

Lymphocytic hypereosinophilic syndrome

ORPHA:314970Clin. sub.

Lymphoid interstitial pneumonia

ORPHA:79128Disease
Not applicable

Lymphomatoid granulomatosis

ORPHA:86869Disease
Not applicable

Lymphomatoid papulosis

ORPHA:98842Disease

Lymphoplasmacytic inflammatory pseudotumor of the liver

ORPHA:555437Clin. sub.

Lymphoplasmacytic lymphoma without IgM production

ORPHA:443159Disease
Not applicable

Lymphoproliferative disease associated with primary immune disease

ORPHA:98291Cat.

Lynch syndrome

ORPHA:144Disease
Autosomal dominant

Lysinuric protein intolerance

ORPHA:470Disease
Autosomal recessive

Lysosomal acid lipase deficiency

ORPHA:275761Disease
Autosomal recessive

Lysosomal acid phosphatase deficiency

ORPHA:35121Disease
Autosomal recessive

Léri-Weill dyschondrosteosis

ORPHA:240Malform.
Autosomal dominant

MADD-related developmental delay-endocrine dysfunction-hypohemoglobinemia syndrome

ORPHA:686495Disease
Autosomal recessive

MAGIC syndrome

ORPHA:324972Disease

MALT lymphoma

ORPHA:52417Disease
Multigenic/multifactorial, Not applicable

MAN1B1-CDG

ORPHA:397941Disease
Autosomal recessive

MAN2B2-CDG

ORPHA:695110Disease
Autosomal recessive