MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

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

Frontal encephalocele

ORPHA:1931Kl. subt.

Frontal fibrosing alopecia

ORPHA:254492Kr.

Frontofacionasal dysplasia

ORPHA:1791Malf.

Frontometaphyseal dysplasia

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

Frontonasal dysplasia

ORPHA:250Kl. gruppe
Not applicable

Frontonasal dysplasia-alopecia-genital anomalies syndrome

ORPHA:228390Malf.
Autosomal recessive

Frontonasal dysplasia-bifid nose-upper limb anomalies syndrome

ORPHA:521308Malf.

Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome

ORPHA:306542Malf.
Autosomal recessive

Frontorhiny

ORPHA:391474Malf.
Autosomal recessive

Frontotemporal dementia

ORPHA:282Kl. gruppe
Autosomal dominant

Frontotemporal dementia with motor neuron disease

ORPHA:275872Kr.
Autosomal dominant

Fructose-1,6-bisphosphatase deficiency

ORPHA:348Kr.
Autosomal recessive

Fryns syndrome

ORPHA:2059Malf.
Autosomal recessive

Fryns-Smeets-Thiry syndrome

ORPHA:2058Malf.

Fuchs endothelial corneal dystrophy

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

Fuchs heterochromic iridocyclitis

ORPHA:263479Kr.

Fucosidosis

ORPHA:349Kr.
Autosomal recessive

Fuhrmann syndrome

ORPHA:2854Malf.
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

Fumaric aciduria

ORPHA:24Kr.
Autosomal recessive

Functional variant of Guillain-Barré syndrome

ORPHA:231419Kl. gruppe
Multigenic/multifactorial, Not applicable

Functioning gonadotropic adenoma

ORPHA:91348Kr.