Disease Index

9,486 diseases
Focal palmoplantar and gingival keratosis
medical condition
MeSH: C536157
focal palmoplantar keratoderma
human disease
focal palmoplantar keratoderma with joint keratoses
human disease
Focal palmoplantar keratoderma with oral mucosal hyperkeratosis
MeSH: C566180
focal stiff limb syndrome
human disease
focal, segmental or multifocal dystonia
Focal Dystonia is a rare neurologic movement disorder characterized by sustained muscle contractions of a single body region, usually producing twisting and repetitive movements or abnormal postures or positions
Foix–Alajouanine syndrome
medical condition
Foix–Chavany–Marie syndrome
Illness
MeSH: C537069
folinic acid-responsive seizures
follicular atrophoderma-basal cell carcinoma
human disease
follicular cholangitis and pancreatitis
human disease
follicular dendritic cell sarcoma
dendritic cell sarcoma cancer that effects the follicular dendritic cells
MeSH: D054740
follicular lymphoma
non-Hodgkin lymphoma that is characterized as an indolent non-Hodgkin's lymphoma and has_material_basis_in follicle center B-cells (centrocytes and centroblasts).
ICD: C82MeSH: D008224
folliculitis decalvans
medical condition
ICD: L66.2
folliculotropic mycosis fungoides
foodborne botulism
human disease
Forney robinson pascoe syndrome
MeSH: C537269
Fountain syndrome
extremely rare multi-systemic genetic disorder characterized by intellectual disability, deafness, skeletal abnormalities and coarse facial features
MeSH: C537270
fourth branchial cleft anomaly
human disease
foveal hypoplasia-optic nerve decussation defect-anterior segment dysgenesis syndrome
human disease
foveal hypoplasia-presenile cataract syndrome
human disease
MeSH: C537858
Fowler syndrome
human disease
MeSH: C565593
FOXG1 syndrome
medical condition
fragile X syndrome
congenital disorder of nervous system
ICD: Q99.2MeSH: D005600
fragile X-associated tremor/ataxia syndrome
Fragile X-associated tremor/ataxia syndrome (FXTAS) is a rare neurodegenerative disorder characterized by adult-onset progressive intention tremor and gait ataxia
MeSH: C564105
Frank–Ter Haar syndrome
human disease
MeSH: C537274
Fraser syndrome
autosomal recessive congenital disorder
MeSH: D058497
Fraser-like syndrome
human disease
MeSH: C565562
Frasier syndrome
Human disease
MeSH: D052159
FRAXE intellectual disability
FRAXE is a form of nonsyndromic X-linked mental retardation (NS-XLMR) characterized by mild intellectual deficit. FRAXE is the most common form of NS-XLMR.
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