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Disease	Synonyms	Description	Articles
Bartholin's gland squamous cell carcinoma	Bartholin gland squamous cell carcinoma;	n_a
Bartholin's gland transitional cell carcinoma	Bartholin gland transitional cell carcinoma;	n_a
Bartter disease	Aldosteronism with hyperplasia of the adrenal cort.. [+] Aldosteronism with hyperplasia of the adrenal cortex; Bartter's syndrome; [-]	n_a	8 articles
Bartter disease type 1	BARTS1; Bartter syndrome type 1; Bartter syndrome .. [+] BARTS1; Bartter syndrome type 1; Bartter syndrome type 1 antenatal; hyperprostaglandin E syndrome 1; hypokalemic alkalosis with hypercalciuria 1 antenatal; [-]	A Bartter disease that has_material_basis_in homoz..[+] A Bartter disease that has_material_basis_in homozygous or compound heterozygous mutation in the sodium-potassium-chloride cotransporter-2 gene (SLC12A1) on chromosome 15q21. [-]	1 articles
Bartter disease type 2	BARTS2; Bartter syndrome type 2; hyperprostaglandi.. [+] BARTS2; Bartter syndrome type 2; hyperprostaglandin E syndrome 2; hypokalemic alkalosis with hypercalciuria 2 antenatal; Bartter syndrome type 2 antenatal; [-]	A Bartter disease that has_material_basis_in homoz..[+] A Bartter disease that has_material_basis_in homozygous or compound heterozygous mutation in the potassium channel ROMK gene (KCNJ1) on chromosome 11q24. [-]	1 articles
Bartter disease type 3	BARTS3; Bartter syndrome type 3; classic Bartter s.. [+] BARTS3; Bartter syndrome type 3; classic Bartter syndrome; [-]	A Bartter disease that has_material_basis_in homoz..[+] A Bartter disease that has_material_basis_in homozygous or compound heterozygous mutation in the kidney chloride channel B gene (CLCNKB) on chromosome 1p36. [-]	2 articles
Bartter disease type 4a	BARTS4A; Bartter syndrome type 4a ; BSND; neonatal.. [+] BARTS4A; Bartter syndrome type 4a ; BSND; neonatal Bartter syndrome with sensorineural deafness; [-]	A Bartter disease that has_material_basis_in homoz..[+] A Bartter disease that has_material_basis_in homozygous or compound heterozygous mutation in the BSND gene on chromosome 1p32. [-]
Bartter disease type 4b	Bartter syndrome, type 4b, digenic; BARTS4B; neona.. [+] Bartter syndrome, type 4b, digenic; BARTS4B; neonatal Bartter syndrome type 4B with sensorineural deafness; [-]	A Bartter disease that has material basis in simul..[+] A Bartter disease that has material basis in simultaneous mutation in both the CLCNKA and CLCNKB genes. [-]
Bartter disease type 5	BARTS5; Bartter syndrome, type 5, antenatal, trans.. [+] BARTS5; Bartter syndrome, type 5, antenatal, transient; [-]	A Bartter disease that has material basis in mutat..[+] A Bartter disease that has material basis in mutation in the MAGED2 gene on chromosome Xp11. [-]
Basilicata-Akhtar syndrome	MRXS36; X-linked syndromic mental retardation 36; .. [+] MRXS36; X-linked syndromic mental retardation 36; X-linked syndromic mental retardation Basilicata-Akhtar type; [-]	A syndromic X-linked intellectual disability chara..[+] A syndromic X-linked intellectual disability characterized by global developmental delay apparent from infancy, feeding difficulties, hypotonia, and poor or absent speech that has_material_basis_in hemizygous or heterozygous mutation in the MSL3 gene on chromosome Xp22.2. [-]
Beare-Stevenson cutis gyrata syndrome		A syndrome that is characterized by cutis gyrata, ..[+] A syndrome that is characterized by cutis gyrata, acanthosis nigricans and craniosynostosis, has_material_basis_in heterozygous mutation in the FGFR2 gene on chromosome 10q26. [-]
Becker disease		A myotonia congenita that is characterized by musc..[+] A myotonia congenita that is characterized by muscle stiffness and an inability of the muscle to relax after voluntary contraction and that has_material_basis_in homozygous or compound heterozygous mutation in the gene encoding skeletal muscle chloride channel-1 (CLCN1) on chromosome 7q34. [-]
Becker muscular dystrophy	benign congenital myopathy; Benign pseudohypertrop.. [+] benign congenital myopathy; Benign pseudohypertrophic muscular dystrophy; [-]	A muscular dystrophy that involves slowly worsenin..[+] A muscular dystrophy that involves slowly worsening muscle weakness of the legs and pelvis, and has_material_basis_in X-linked recessive inheritance of mutation in the dystrophin gene on chromosome Xp21. [-]
Beckwith-Wiedemann syndrome		A syndrome characterized by overgrowth (macrosomia..[+] A syndrome characterized by overgrowth (macrosomia), an increased risk of childhood cancer and congenital malformations. [-]
Beemer-Langer syndrome	type IV short rib polydactyly syndrome (disorder);.. [+] type IV short rib polydactyly syndrome (disorder); type IV short rib polydactyly syndrome; [-]	A syndrome that results_in multiple congenital ano..[+] A syndrome that results_in multiple congenital anomalies, including hydrops fetalis, facial and visceral abnormalities, short ribs, and short limbs without polydactyly. [-]
Behcet's disease	Adamantiades-Behcet disease; Behcet syndrome; Behc.. [+] Adamantiades-Behcet disease; Behcet syndrome; Behcet's syndrome; Behet's syndrome; triple symptom complex; [-]	A vasculitis that is characterized by an autoimmun..[+] A vasculitis that is characterized by an autoimmune mediated inflammation of the blood vessels throughout the body leading to ulcerations on the mouth and sometimes the genitals, notorious for causing hypopyon uveitis. [-]
Behcet's syndrome arthropathy	Arthropathy in Behcet's syndrome involving forearm.. [+] Arthropathy in Behcet's syndrome involving forearm; Arthropathy in Behcet's syndrome involving hand; Arthropathy in Behcet's syndrome involving multiple sites; Arthropathy in Behcet's syndrome involving shoulder region; Behcet syndrome arthropathy; Arthropathy in Behcet's syndrome involving ankle and foot; Arthropathy in Behcet's syndrome involving pelvic region and thigh; Arthropathy in Behcet's syndrome involving lower leg; Arthropathy in Behcet's syndrome involving upper arm; [-]	n_a
Behr syndrome	Abortive cerebellar ataxia (BEHRS); optic atrophy .. [+] Abortive cerebellar ataxia (BEHRS); optic atrophy in early childhood, associated with ataxia, spasticity, mental retardation, and posterior column sensory loss; BEHRS; optic atrophy, infantile hereditary, Behr complicated form of; [-]	A nervous system disease characterized by early-on..[+] A nervous system disease characterized by early-onset optic atrophy, ataxia, pyramidal signs, spasticity, and intellectual disability that has_material_basis_in homozygous or compound heterozygous mutation in the OPA1 gene on chromosome 3q29. [-]
Bell's palsy	Bell palsy; Bell's (facial) palsy;	A facial paralysis resulting from dysfunction in t..[+] A facial paralysis resulting from dysfunction in the cranial nerve VII (facial nerve). [-]
Bernard-Soulier syndrome	Bernard - Soulier thrombopathy; Bernard Soulier sy.. [+] Bernard - Soulier thrombopathy; Bernard Soulier syndrome; Thrombopathy, Bernard-Soulier; Giant platelet syndrome (disorder); Giant platelet syndrome; Hemorrhagic dystrophic thrombocytopenia; [-]	A blood coagulation disease characterized by autos..[+] A blood coagulation disease characterized by autosomal recessive inheritance of mucosal bleeding, purpuric skin bleeding, epistaxis, and menorrhagia with prolonged bleeding times, enlarged platelets and absence of platelet aggregation in response to von Willebrand factor that has_material_basis_in mutation in the GP1BA gene, the GP1BB gene, or the GP9 gene which are subunits of the platelet membrane von Willebrand factor receptor complex, glycoprotein Ib. [-]

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