MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes

Macrodactyly of toes, unilateral

ORPHA:295243Clin. sub.
Autosomal dominant

Macrophage activation syndrome

ORPHA:158061Clinical syndrome

Macrophagic myofasciitis

ORPHA:592Disease
Not applicable

Macrosomia-microphthalmia-cleft palate syndrome

ORPHA:2432Malform.

Macrostomia-preauricular tags-external ophthalmoplegia syndrome

ORPHA:83619Malform.
Autosomal dominant

Macrothrombocytopenia with mitral valve insufficiency

ORPHA:220448Disease

Macular coloboma-cleft palate-hallux valgus syndrome

ORPHA:91494Malform.
Autosomal recessive

Macular corneal dystrophy

ORPHA:98969Disease
Autosomal recessive

Maculopapular cutaneous mastocytosis

ORPHA:79457Disease
Not applicable

Madras motor neuron disease

ORPHA:137867Disease
Not applicable, X-linked recessive

Maffucci syndrome

ORPHA:163634Disease
Not applicable

Majeed syndrome

ORPHA:77297Disease
Autosomal recessive

Mal de Meleda

ORPHA:87503Disease
Autosomal recessive

Mal de débarquement

ORPHA:210272Clinical syndrome
Not applicable

Malakoplakia

ORPHA:556Disease
Unknown

Malan overgrowth syndrome

ORPHA:420179Malform.
Autosomal dominant, Unknown

Malaria

ORPHA:673Disease
Not applicable

Male hypergonadotropic hypogonadism-intellectual disability-skeletal anomalies syndrome

ORPHA:2234Malform.
Unknown

Male infertility due to acephalic spermatozoa

ORPHA:529970Clin. sub.
Autosomal recessive

Male infertility due to globozoospermia

ORPHA:171709Clin. sub.
Autosomal recessive

Male infertility due to large-headed multiflagellar polyploid spermatozoa

ORPHA:137893Clin. sub.
Autosomal recessive

Male infertility with azoospermia or oligozoospermia due to single gene mutation

ORPHA:399805Disease
Autosomal dominant, Autosomal recessive, X-linked recessive

Male infertility with teratozoospermia due to single gene mutation

ORPHA:399808Disease

Malformation of the neurenteric canal, spinal cord and column

ORPHA:268843Cat.