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

MYT1L-related developmental delay-intellectual disability-obesity syndrome

ORPHA:647799Kr.
Autosomal dominant

Macrocephaly-intellectual disability-autism syndrome

ORPHA:210548Kr.
Autosomal dominant

Macrophagic myofasciitis

ORPHA:592Kr.
Not applicable

Macrothrombocytopenia with mitral valve insufficiency

ORPHA:220448Kr.

Macular corneal dystrophy

ORPHA:98969Kr.
Autosomal recessive

Maculopapular cutaneous mastocytosis

ORPHA:79457Kr.
Not applicable

Madras motor neuron disease

ORPHA:137867Kr.
Not applicable, X-linked recessive

Maffucci syndrome

ORPHA:163634Kr.
Not applicable

Majeed syndrome

ORPHA:77297Kr.
Autosomal recessive

Mal de Meleda

ORPHA:87503Kr.
Autosomal recessive

Malakoplakia

ORPHA:556Kr.
Unknown

Malaria

ORPHA:673Kr.
Not applicable

Male infertility with azoospermia or oligozoospermia due to single gene mutation

ORPHA:399805Kr.
Autosomal dominant, Autosomal recessive, X-linked recessive

Male infertility with teratozoospermia due to single gene mutation

ORPHA:399808Kr.

Malignant Sertoli-Leydig cell tumor of the ovary

ORPHA:99916Kr.

Malignant epithelial tumor of salivary glands

ORPHA:276145Kr.
Not applicable

Malignant germ cell tumor of the corpus uteri

ORPHA:213751Kr.

Malignant granulosa cell tumor of the ovary

ORPHA:99915Kr.
Multigenic/multifactorial

Malignant hyperthermia of anesthesia

ORPHA:423Kr.
Autosomal dominant

Malignant melanoma of the mucosa

ORPHA:168999Kr.

Malignant mixed Müllerian tumor of the ovary

ORPHA:213512Kr.

Malignant non-dysgerminomatous germ cell tumor of ovary

ORPHA:206538Kr.
Unknown

Malignant peripheral nerve sheath tumor

ORPHA:3148Kr.
Not applicable

Malignant peritoneal mesothelioma

ORPHA:168811Kr.
Multigenic/multifactorial, Not applicable