MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes
218 diseases matched (Clin. grp.) Reset

Large granular lymphocyte leukemia

ORPHA:512034Clin. grp.

Lateral facial cleft

ORPHA:141269Clin. grp.

Lichen myxedematosus

ORPHA:402007Clin. grp.

Limb-girdle muscular dystrophy

ORPHA:263Clin. grp.
Autosomal dominant, Autosomal recessive

Lissencephaly with cerebellar hypoplasia

ORPHA:86823Clin. grp.

Localized lipodystrophy

ORPHA:79088Clin. grp.
Unknown

Marginal papular palmoplantar keratoderma

ORPHA:307995Clin. grp.
Autosomal dominant

Marginal zone lymphoma

ORPHA:300912Clin. grp.

Median facial cleft

ORPHA:141234Clin. grp.

Mendelian susceptibility to mycobacterial diseases

ORPHA:748Clin. grp.
Autosomal dominant, Autosomal recessive, X-linked recessive

Methylmalonic acidemia without homocystinuria

ORPHA:293355Clin. grp.
Autosomal dominant, Autosomal recessive, X-linked dominant

Mitochondrial DNA depletion syndrome, encephalomyopathic form

ORPHA:254803Clin. grp.
Autosomal recessive

Mitochondrial DNA depletion syndrome, hepatocerebral form

ORPHA:254871Clin. grp.
Autosomal recessive

Mitochondrial DNA-related mitochondrial myopathy

ORPHA:254788Clin. grp.
Mitochondrial inheritance

Multiple carboxylase deficiency

ORPHA:148Clin. grp.
Autosomal recessive

Multiple endocrine neoplasia

ORPHA:276161Clin. grp.
Autosomal dominant, Not applicable

Multiple epiphyseal dysplasia

ORPHA:251Clin. grp.
Autosomal dominant, Autosomal recessive

Multiple mitochondrial dysfunctions syndrome

ORPHA:289573Clin. grp.
Autosomal recessive

Mycosis fungoides and variants

ORPHA:178566Clin. grp.
Not applicable

Myelocystocele

ORPHA:268813Clin. grp.
Multigenic/multifactorial, Not applicable

Myelodysplastic syndrome

ORPHA:52688Clin. grp.

Myelodysplastic/myeloproliferative disease

ORPHA:98275Clin. grp.

Myeloproliferative neoplasm

ORPHA:98274Clin. grp.

Myotonic dystrophy

ORPHA:206647Clin. grp.