MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

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

Extraskeletal Ewing sarcoma

ORPHA:370334Kr.
Not applicable

Extraskeletal myxoid chondrosarcoma

ORPHA:209916Kr.
Not applicable

Extrasystoles-short stature-hyperpigmentation-microcephaly syndrome

ORPHA:1964Malf.
Autosomal dominant

Eyebrow duplication-syndactyly syndrome

ORPHA:3172Malf.
Autosomal recessive

Eyelid sebaceous carcinoma

ORPHA:658590Kr.

F12-associated cold autoinflammatory syndrome

ORPHA:617919Kr.
Autosomal dominant

F12-related hereditary angioedema with normal C1Inh

ORPHA:100054Kl. subt.
Autosomal dominant

FADD-related immunodeficiency

ORPHA:306550Kr.
Autosomal recessive

FASTKD2-related infantile mitochondrial encephalomyopathy

ORPHA:166105Kr.
Autosomal recessive

FATCO syndrome

ORPHA:2492Malf.

FBLN1-related developmental delay-central nervous system anomaly-syndactyly syndrome

ORPHA:404451Malf.
Autosomal recessive

FG syndrome type 1

ORPHA:93932Kr.
X-linked recessive

FGFR2-related bent bone dysplasia

ORPHA:313855Kr.
Autosomal dominant

FGFR3-related chondrodysplasia

ORPHA:93420Kat.

FKRP-related limb-girdle muscular dystrophy R9

ORPHA:34515Kr.
Autosomal recessive

FLNA-related X-linked myxomatous valvular dysplasia

ORPHA:555877Morph.
X-linked recessive

FLNC-related handgrip and calf weakness-distal myopathy

ORPHA:63273Kr.
Autosomal dominant

FLOTCH syndrome

ORPHA:2045Kr.

FOXG1 syndrome

ORPHA:561854Kr.

FOXG1 syndrome due to 14q12 microdeletion

ORPHA:261144Kl. subt.
Not applicable

FOXG1 syndrome due to intragenic alteration

ORPHA:598164Kl. subt.
Autosomal dominant

FOXP1 Syndrome

ORPHA:391372Malf.
Autosomal dominant

FRAXE intellectual disability

ORPHA:100973Kr.
X-linked recessive

FRAXF syndrome

ORPHA:100974Kr.
Unknown