Disease Index

9,486 diseases
functional variant of Guillain-Barre syndrome
human disease
functioning gonadotropic adenoma
functioning pituitary adenoma
Human disease
functionless pituitary adenoma
Human disease
fundus albipunctatus
fundus dystrophy that is characterized by discrete uniform white dots over the entire fundus with greatest density in the midperiphery and no macular involvement
MeSH: C562733
fundus dystrophy
human disease
MeSH: D058499
fundus pulverulentus
human disease
fungal infectious disease
disease caused by fungi to animals or humans
MeSH: D009181
fungal myositis
human disease
furuncular myiasis
Furuncular myiasis in humans is caused by two species: the Cayor worm (larvae of the African tumbu fly Cordylobia anthropophaga) and the larvae of the human botfly (Dermatobia hominis)
MeSH: C538194
fusariosis
Human disease
MeSH: D060585
fused mandibular incisors
MeSH: C535997
GABA aminotransferase deficiency
Human disease
MeSH: C535407
Gabriele-de Vries syndrome
human disease
galactokinase deficiency
galactosemia that involves an accumulation of galactose and galactitol secondary to the decreased conversion of galactose to galactose-1-phosphate by galactokinase
galactose epimerase deficiency
human disease
galactose-1-phosphate uridylyltransferase deficiency
human disease
ICD: E74.2
galactosemia
carbohydrate metabolic disorder that involves a defect in galactose metabolism resulting in toxic levels of galactose 1-phosphate in various tissues
MeSH: D005693
galactosialidosis
rare disease
ICD: E77.1MeSH: C536411
gallbladder neuroendocrine neoplasm
neoplasm with neuroendocrine differentiation that arises from the gallbladder. It includes well differentiated neuroendocrine tumors (low and intermediate grade) and poorly differentiated neuroendocrine carcinomas (high grade)
gallbladder neuroendocrine tumor, grade 1/2
well differentiated, low or intermediate grade tumor with neuroendocrine differentiation that arises from the gallbladder
Galloway-Mowat syndrome
autosomal recessive disease characterized by is a rare autosomal recessive disease, characterized by microcephaly with brain anomalies including CA in some cases, intellectual disability, and early-infantile-onset nephrotic syndrome
MeSH: C537548
Galloway-Mowat syndrome 2
human disease
Galloway-Mowat syndrome 3
human disease
Galloway-Mowat syndrome 4
human disease
Galloway-Mowat syndrome 5
human disease
gamma chain deficiency
immunodeficiency disorder in which the body produces very few T cells and NK cells
ICD: D80.0MeSH: D053632
gamma heavy chain disease
heavy chain disease that results from an overproduction of gamma antibody (IgG)
gamma-glutamylcysteine synthetase deficiency
Gamma-glutamylcysteine synthetase deficiency is principally characterized by hemolytic anemia, (usually rather mild), however, the presence of neurological symptoms has also been reported
MeSH: C565557
Gamstorp-Wohlfart syndrome
syndrome characterized by progressive weakness and atrophy of muscles in feet, legs and hands. In some patients the syndrome also causes decreased sensitivity to touch, heat or cold, particularly in the lower arms or legs
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