Becker nevus syndrome is a condition characterized by the presence of a distinctive, often hyperpigmented and sometimes hairy, skin patch (Becker nevu...

Beck-Fahrner syndrome is a disorder that falls within the spectrum of chromatin-modifying conditions and primarily affects the nervous system as well...

Beckwith-Wiedemann syndrome (BWS) is a genetic overgrowth disorder marked by congenital malformations, an increased predisposition to tumors, and a ra...

Beckwith-Wiedemann syndrome due to 11p15 microdeletion is a condition that arises from disturbances in the imprinting process, where gene expression d...

Beckwith-Wiedemann syndrome due to 11p15 microduplication is an imprinting disorder in which alterations in gene expression depend on the parent-of-or...

Beckwith-Wiedemann syndrome due to 11p15 translocation/inversion is a condition affecting growth regulation, resulting from abnormalities in the impri...

Beckwith-Wiedemann syndrome is an imprinting disorder characterized by abnormal growth regulation and a predisposition to various complications. Altho...

Beckwith-Wiedemann syndrome due to imprinting defect of 11p15 is a congenital condition primarily characterized by disturbances in growth regulation t...

Information about overview is currently limited for this condition.

Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11 is a congenital condition that results from an imprinting error, in wh...

Beemer-Ertbruggen syndrome is a lethal malformation syndrome characterized by severe structural abnormalities including hydrocephalus, cardiac malform...

Beemer-Langer syndrome is an extremely rare skeletal dysplasia in the spectrum of short rib-polydactyly syndromes that typically presents prenatally o...

Behavioral variant of frontotemporal dementia (bv-FTD) is characterized by progressive behavioral impairment and a decline in executive function, prim...

Behcet disease is a chronic, relapsing, multisystemic vasculitis that primarily affects mucocutaneous tissues, as well as joints, blood vessels, the e...

Behrens Baumann dust syndrome is a condition with limited clinical data that appears to involve developmental anomalies affecting the ocular and cereb...

Behr syndrome is an inherited disorder that primarily affects both the eyes and the nervous system, with early-onset optic atrophy being a hallmark fe...

bejel is an extremely rare condition. It is a chronic skin and tissue disease caused by infection with the endemicum subspecies of the spirochete Trep...

Bencze syndrome is a malformation syndrome characterized by abnormal overgrowth of the facial skeleton and soft tissues, leading to mild facial asymme...

benign adrenal gland pheochromocytoma is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited...

Benign adult familial myoclonic epilepsy is an extremely rare condition. Because few cases have been documented, detailed clinical information is limi...