MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

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

Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency

ORPHA:314637Kr.
Unknown

Mitochondrial membrane protein-associated neurodegeneration

ORPHA:289560Kr.
Autosomal recessive

Mitochondrial myopathy and sideroblastic anemia

ORPHA:2598Kr.
Autosomal recessive

Mitochondrial myopathy with reversible cytochrome C oxidase deficiency

ORPHA:254864Kr.
Mitochondrial inheritance

Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome

ORPHA:502423Kr.
Autosomal dominant

Mitochondrial myopathy-lactic acidosis-deafness syndrome

ORPHA:2597Kr.
No data available

Mitochondrial neurogastrointestinal encephalomyopathy

ORPHA:298Kr.
Autosomal recessive

Mitochondrial oxidative phosphorylation disorder due to nuclear DNA anomalies

ORPHA:2443Kat.
Autosomal recessive

Mitochondrial pyruvate carrier deficiency

ORPHA:447784Kr.
Autosomal recessive

Mitochondrial short-chain enoyl-CoA hydratase 1 deficiency

ORPHA:653880Kr.
Autosomal recessive

Mitochondrial trifunctional protein deficiency

ORPHA:746Kr.
Autosomal recessive

Mixed connective tissue disease

ORPHA:809Kr.
Multigenic/multifactorial

Mixed cryoglobulinemia type II

ORPHA:93554Ätl. subt.

Mixed cryoglobulinemia type III

ORPHA:93555Ätl. subt.

Mixed cystic lymphatic malformation

ORPHA:458792Malf.
Not applicable

Mixed germ cell tumor

ORPHA:180234Kr.
Not applicable

Mixed phenotype acute leukemia

ORPHA:530995Kr.

Mixed phenotype acute leukemia with t(9;22)(q34.1;q11.2)

ORPHA:589534Ätl. subt.
Not applicable

Mixed phenotype acute leukemia with t(v;11q23.3)

ORPHA:589595Ätl. subt.
Not applicable

Mixed sclerosing bone dystrophy with extra-skeletal manifestations

ORPHA:324364Kr.

Mixed-type autoimmune hemolytic anemia

ORPHA:90036Kr.
Multigenic/multifactorial

Miyoshi myopathy

ORPHA:45448Kr.
Autosomal recessive

Moderate and severe traumatic brain injury

ORPHA:90056spez. Sit.
Not applicable

Moderate hemophilia A

ORPHA:169805Kl. subt.
X-linked recessive