Disease Index
9,486 diseasesfatty acid hydroxylase-associated neurodegeneration
fatty acid oxidation and ketogenesis disorder with dilated cardiomyopathy
human disease
fatty acid oxidation and ketogenesis disorder with hypertrophic cardiomyopathy
human disease
favism, susceptibility to
human disease
Fazio-Londe disease
a very rare inherited motor neuron disease of children and young adults
ICD: G12.1
FBLN1-related developmental delay-central nervous system anomaly-syndactyly syndrome
human disease
febrile infection-related epilepsy syndrome
an explosive-onset, potentially fatal acute epileptic encephalopathy that develops in previously healthy children and adolescents following the onset of a non-specific febrile illness
ICD: G40.5
febrile neutrophilic dermatosis
skin disease
ICD: L98.2MeSH: D016463
Fechtner syndrome
genetic disorder
Feingold syndrome
autosomal dominant disease characterized by variable combinations of microcephaly, limb malformations, esophageal and duodenal atresias, and learning disability/mental retardation
MeSH: C537734
Felty's syndrome
syndrome that results in rheumatoid arthritis, splenomegaly and neutropenia
MeSH: D005258
female infertility due to an implantation defect
human disease
female infertility due to an implantation defect of genetic origin
human disease
female infertility due to fertilization defect
human disease
female infertility due to gonadal dysgenesis
human disease
female infertility due to zona pellucida defect
human disease
female reproductive organ cancer
human disease
femoral agenesis/hypoplasia
Congenital short femur is a rare malformation of variable severity ranging from mild hypoplasia to complete absence of the femur
femoral agenesis/hypoplasia, bilateral
human disease
femoral agenesis/hypoplasia, unilateral
human disease
Femoral-facial syndrome
Femoral-facial syndrome is characterized by predominant femoral hypoplasia (bilateral or unilateral) and unusual facies
MeSH: C537916
Femur fibula ulna syndrome
medical condition
ICD: Q74.8MeSH: C537918
Ferguson-Smith tumor
human disease
MeSH: C536150
ferro-cerebro-cutaneous syndrome
human disease
fetal akinesia deformation sequence
human disease
fetal akinesia-cerebral and retinal hemorrhage syndrome
fetal alcohol syndrome
severe form of fetal alcohol spectrum disorder
ICD: Q86.0
fetal anticonvulsant syndrome
human disease
fetal brain disruption sequence
human disease
fetal carbamazepine syndrome
exposure to carbamazepine, in combination with valproate, has been associated with significant developmental delay (particularly affecting verbal intelligence) and a high rate of congenital anomalies