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

Follicular cholangitis and pancreatitis

ORPHA:300552Kr.
Unknown

Follicular dendritic cell sarcoma

ORPHA:86902Kr.

Follicular lymphoma

ORPHA:545Kr.
Multigenic/multifactorial, Not applicable

Folliculotropic mycosis fungoides

ORPHA:178512Kr.
Not applicable

Fontan-associated liver disease

ORPHA:699068Kr.
Not applicable

Formiminoglutamic aciduria

ORPHA:51208Kr.
Autosomal recessive

Foveal hypoplasia-optic nerve decussation defect-anterior segment dysgenesis syndrome

ORPHA:397618Kr.
Autosomal recessive

Foveal hypoplasia-presenile cataract syndrome

ORPHA:2253Kr.
Autosomal dominant

Fowler urethral sphincter dysfunction syndrome

ORPHA:2795Kr.
Unknown

Fragile X-associated primary ovarian insufficiency

ORPHA:642691Kr.

Frank-Ter Haar syndrome

ORPHA:137834Kr.
Autosomal recessive

Frasier syndrome

ORPHA:347Kr.
Autosomal dominant

Free sialic acid storage disease

ORPHA:834Kr.
Autosomal recessive

Friedreich ataxia

ORPHA:95Kr.
Autosomal recessive

Frontal fibrosing alopecia

ORPHA:254492Kr.

Frontometaphyseal dysplasia

ORPHA:1826Kr.
Autosomal dominant, X-linked dominant

Frontotemporal dementia with motor neuron disease

ORPHA:275872Kr.
Autosomal dominant

Fructose-1,6-bisphosphatase deficiency

ORPHA:348Kr.
Autosomal recessive

Fuchs endothelial corneal dystrophy

ORPHA:98974Kr.
Autosomal dominant, Multigenic/multifactorial, Not applicable

Fuchs heterochromic iridocyclitis

ORPHA:263479Kr.

Fucosidosis

ORPHA:349Kr.
Autosomal recessive

Fukutin-related limb-girdle muscular dystrophy R13

ORPHA:206554Kr.
Autosomal recessive

Full NF2-related schwannomatosis

ORPHA:637Kr.
Autosomal dominant

Full schwannomatosis

ORPHA:93921Kr.
Autosomal dominant