MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes
1,772 diseases matched (Malform.) Reset

Femur-fibula-ulna complex

ORPHA:2019Malform.
Not applicable

Fetal akinesia deformation sequence

ORPHA:994Malform.
Autosomal recessive

Fetal alcohol syndrome

ORPHA:1915Malform.
Not applicable

Fetal carbamazepine syndrome

ORPHA:370076Malform.
Not applicable

Fetal encasement syndrome

ORPHA:465824Malform.
Autosomal recessive

Fetal hydantoin syndrome

ORPHA:1912Malform.
Not applicable

Fetal iodine syndrome

ORPHA:1910Malform.
Not applicable

Fetal methylmercury syndrome

ORPHA:1917Malform.
Not applicable

Fetal minoxidil syndrome

ORPHA:1918Malform.
Not applicable

Fetal parvovirus syndrome

ORPHA:295Malform.
Not applicable

Fetal trimethadione syndrome

ORPHA:1913Malform.
Not applicable

Fetal valproate spectrum disorder

ORPHA:1906Malform.
Not applicable

Fibrous dysplasia of bone

ORPHA:249Malform.
Not applicable

Fibular aplasia-complex brachydactyly syndrome

ORPHA:2639Malform.
Autosomal recessive

Fibular aplasia-ectrodactyly syndrome

ORPHA:1118Malform.
Autosomal dominant

Fibular dimelia-diplopodia syndrome

ORPHA:1757Malform.
Not applicable

Fibulo-ulnar hypoplasia-renal anomalies syndrome

ORPHA:2256Malform.

Filippi syndrome

ORPHA:3255Malform.
Autosomal recessive

Finger hyperphalangy-toe anomalies-severe pectus excavatum syndrome

ORPHA:369979Malform.

Flat face-microstomia-ear anomaly syndrome

ORPHA:1968Malform.
Unknown

Floating-Harbor syndrome

ORPHA:2044Malform.
Autosomal dominant

Focal dermal hypoplasia

ORPHA:2092Malform.
X-linked dominant

Focal facial dermal dysplasia

ORPHA:398166Malform.
Autosomal dominant, Autosomal recessive

Foix-Chavany-Marie syndrome

ORPHA:2048Malform.
Not applicable