Disease Index
9,486 diseasesBeckwith-Wiedemann syndrome due to imprinting defect of 11p15
human disease
Beckwith-Wiedemann syndrome due to NSD1 mutation
human disease
Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11
human disease
Beemer-Ertbruggen syndrome
MeSH: C537668
Beemer-Langer syndrome
syndrome that results in multiple congenital anomalies, including hydrops fetalis, facial and visceral abnormalities, short ribs, and short limbs without polydactyly
MeSH: C537599
behavioral variant of frontotemporal dementia
Behavioral variant of frontotemporal dementia (bv-FTD) is a form of frontotemporal dementia (FTD; see this term), characterized by progressive behavioral impairment and a decline in executive function with frontal lobe-predominant atrophy
Behçet's disease
rare immune-mediated small-vessel systemic vasculitis in humans
MeSH: D001528
Behr syndrome
medical condition
MeSH: C537669
Bellini duct carcinoma
disease
Bencze syndrome
MeSH: C564199
benign adult familial myoclonic epilepsy
human disease
benign cephalic histiocytosis
human disease
ICD: D76.3
benign concentric annular macular dystrophy
MeSH: C537833
benign ductal tumor of breast
human disease
benign epilepsy with centrotemporal spikes
the most common epilepsy syndrome in childhood which usually subsides with age
ICD: G40.0MeSH: D019305
benign epithelial tumor of salivary glands
human disease
benign exophthalmos syndrome
Benign exophthalmos syndrome is characterised by slowly progressive unilateral exophthalmos and ipsilateral mucosal turbinate hypertrophy, without intraorbital or intranasal lesions
benign familial infantile epilepsy
infancy electroclinical syndrome that is characterized by convulsions, with onset at age 3 to 12 months
ICD: G40.3MeSH: C565296
benign familial neonatal epilepsy
Human disease
ICD: G40.3
benign familial nocturnal alternating hemiplegia of childhood
human disease
benign focal seizures of adolescence
human disease
benign idiopathic neonatal seizures
human disease
Benign infantile epilepsy
human disease
benign infantile focal epilepsy with midline spikes and wave during sleep
human disease
benign infantile seizures associated with mild gastroenteritis
human disease
benign metanephric tumour
human disease
benign neonatal seizures
Human disease
MeSH: D020936
benign non-familial infantile seizures
human disease
benign occipital epilepsy
human disease
benign paroxysmal torticollis
rare functional disorder characterised by recurrent episodes of torticollic posturing of the head (inclination or tilting of the head to one side) in healthy children