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

Leber hereditary optic neuropathy

ORPHA:104Kr.
Mitochondrial inheritance

Leber plus disease

ORPHA:99718Kr.
Mitochondrial inheritance

Ledderhose disease

ORPHA:199251Kr.

Left ventricular noncompaction

ORPHA:54260Kr.
Autosomal dominant, Autosomal recessive, Mitochondrial inheritance, X-linked recessive

Legg-Calvé-Perthes disease

ORPHA:2380Kr.
Autosomal dominant, Multigenic/multifactorial

Legionnaires disease

ORPHA:549Kr.
Not applicable

Leigh syndrome

ORPHA:506Kr.
Autosomal recessive, Mitochondrial inheritance, X-linked recessive

Leiomyosarcoma

ORPHA:64720Kr.
Not applicable

Leiomyosarcoma of the cervix uteri

ORPHA:213807Kr.

Leishmaniasis

ORPHA:507Kr.
Not applicable

Lemierre syndrome

ORPHA:137839Kr.

Lennox-Gastaut syndrome

ORPHA:2382Kr.
Autosomal dominant, Multigenic/multifactorial, Not applicable

Leprosy

ORPHA:548Kr.
Multigenic/multifactorial

Leptospirosis

ORPHA:509Kr.
Not applicable

Lesch-Nyhan syndrome

ORPHA:510Kr.
X-linked recessive

Lethal acantholytic erosive disorder

ORPHA:158687Kr.
Autosomal recessive

Lethal arteriopathy syndrome due to fibulin-4 deficiency

ORPHA:314718Kr.
Autosomal recessive

Lethal ataxia with deafness and optic atrophy

ORPHA:1187Kr.
X-linked recessive

Lethal infantile mitochondrial myopathy

ORPHA:254857Kr.
Mitochondrial inheritance

Lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome

ORPHA:478049Kr.
Autosomal recessive

Leukocyte adhesion deficiency

ORPHA:2968Kr.
Autosomal recessive

Leukoencephalopathy with bilateral anterior temporal lobe cysts

ORPHA:139444Kr.
Unknown

Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome

ORPHA:137898Kr.
Autosomal recessive

Leukoencephalopathy with calcifications and cysts

ORPHA:542310Kr.
Autosomal recessive