MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes

Extraskeletal Ewing sarcoma

ORPHA:370334Disease
Not applicable

Extraskeletal myxoid chondrosarcoma

ORPHA:209916Disease
Not applicable

Extrasystoles-short stature-hyperpigmentation-microcephaly syndrome

ORPHA:1964Malform.
Autosomal dominant

Eyebrow duplication-syndactyly syndrome

ORPHA:3172Malform.
Autosomal recessive

Eyelid sebaceous carcinoma

ORPHA:658590Disease

F12-associated cold autoinflammatory syndrome

ORPHA:617919Disease
Autosomal dominant

F12-related hereditary angioedema with normal C1Inh

ORPHA:100054Clin. sub.
Autosomal dominant

FADD-related immunodeficiency

ORPHA:306550Disease
Autosomal recessive

FASTKD2-related infantile mitochondrial encephalomyopathy

ORPHA:166105Disease
Autosomal recessive

FATCO syndrome

ORPHA:2492Malform.

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

ORPHA:404451Malform.
Autosomal recessive

FG syndrome type 1

ORPHA:93932Disease
X-linked recessive

FGFR2-related bent bone dysplasia

ORPHA:313855Disease
Autosomal dominant

FGFR3-related chondrodysplasia

ORPHA:93420Cat.

FKRP-related limb-girdle muscular dystrophy R9

ORPHA:34515Disease
Autosomal recessive

FLNA-related X-linked myxomatous valvular dysplasia

ORPHA:555877Morph.
X-linked recessive

FLNC-related handgrip and calf weakness-distal myopathy

ORPHA:63273Disease
Autosomal dominant

FLOTCH syndrome

ORPHA:2045Disease

FOXG1 syndrome

ORPHA:561854Disease

FOXG1 syndrome due to 14q12 microdeletion

ORPHA:261144Clin. sub.
Not applicable

FOXG1 syndrome due to intragenic alteration

ORPHA:598164Clin. sub.
Autosomal dominant

FOXP1 Syndrome

ORPHA:391372Malform.
Autosomal dominant

FRAXE intellectual disability

ORPHA:100973Disease
X-linked recessive

FRAXF syndrome

ORPHA:100974Disease
Unknown