Disease Index

9,486 diseases
FRAXF syndrome
Freire-Maia odontotrichomelic syndrome
human disease
MeSH: C535637
French Canadian Leigh disease
human disease
Fried syndrome
Fried's tooth and nail syndrome
human disease
Friedreich ataxia
Human disease
ICD: G11.1MeSH: D005621
frontal encephalocele
human disease
frontal fibrosing alopecia
Frontal fibrosing alopecia (FFA) is a rare variant of lichen planopilaris (see this term) characterized by symmetrical, progressive, band-like anterior hair loss of the scalp
Frontofacionasal dysplasia
MeSH: C538063
frontometaphyseal dysplasia
human disease
ICD: Q78.5MeSH: C538064
frontonasal arteriovenous malformation
human disease
frontonasal dysplasia Klippel–Feil syndrome
human disease
frontonasal dysplasia with alopecia and genital anomaly
Frontonasal dysplasia with alopecia and genital anomaly is a new phenotype of frontonasal dysplasia associated with total alopecia and hypogonadism
frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome
human disease
Frontorhiny
frontotemporal degeneration with dementia
human disease
frontotemporal dementia
medical condition
ICD: G31.0MeSH: D057180
frontotemporal dementia, right temporal atrophy variant
frontotemporal neurodegeneration with movement disorder
human disease
fructose-1,6-bisphosphatase deficiency
carbohydrate metabolic disorder that has material basis in a deficiency of fructose-1,6-bisphosphatase resulting in hypoglycemia and metabolic acidosis on fasting due to insufficient fructose bisphosphatase for gluconeogenesis
MeSH: D015319
Fryns syndrome
disease
ICD: Q87.8MeSH: C538070
Fryns-Smeets-Thiry syndrome
human disease
Fuchs' endothelial dystrophy
corneal dystrophy characterized by accumulation of focal outgrowths (guttae) and thickening of Descemet's membrane, leading to corneal edema and loss of vision
MeSH: D005642
Fuchs' heterochromic uveitis
syndrome that is a chronic unilateral (or rarely bilateral) iridocyclitis appearing with the triad of heterochromia, predisposition to cataracts and glaucoma, and keratitic percipitates on the posterior corneal surface
fucosidosis
Human disease
MeSH: D005645
Fuhrmann syndrome
Fuhrmann syndrome is mainly characterized by bowing of the femora, aplasia or hypoplasia of the fibulae and poly-, oligo-, and syndactyly
MeSH: C538189
Fukuyama congenital muscular dystrophy
Human disease
Fulminant viral hepatitis
fumarase deficiency
rare disease
MeSH: C538191
functional neutrophil defect
human disease
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