Disease Search
- Babesiosis
- Baetz-Greenwalt Syndrome
- Bagatelle Cassidy Syndrome
- Bairnsdale ulcer
- Balantidiasis
- Balkan endemic nephropathy
- Baller-Gerold syndrome
- Balo disease
- Balo's concentric sclerosis
- Bamforth Syndrome
- Band-like calcification with simplified gyration and polymicrogyria
- BANF Acoustic Neurinoma
- Bannayan-Riley-Ruvalcaba Syndrome
- Banti's Syndrome
- Bantu siderosis
- Baraitser Brett Piesowicz Syndrome
- Baraitser Rodeck Garner Syndrome
- BARAITSER-WINTER SYNDROME 2
- Barakat Syndrome
- Barber Say Syndrome
- Bardet-Biedl Syndrome
- Bare lymphoccyte syndrome, Type I
- Bare Lymphocyte Syndrome
- Bare Lymphocyte Syndrome 2
- Bare lymphocyte syndrome type 1
- Baritosis
- Baroreflex failure
- Barraquer-Simons Syndrome
- Barre Lieou Syndrome
- Barrett syndrome
- Barrett's Esophagus
- Bart Pumphrey syndrome
- Barth syndrome
- Bartholin cyst
- Bartholin's cyst
- Bartholin's gland cyst
- Bartter Syndrome
- Bartter Syndrome Type 3
- Bartter's Syndrome
- Basal cell carcinoma
- Basal Cell Carcinoma Nevus Syndrome
- Basal ganglia calcification idiopathic childhood-onset
- Basal ganglia calcification, idiopathic, 3
- Basal Ganglia Disease, Biotin-Responsive
- Basal laminar drusen
- Basaloid follicular hamartoma
- Basan Syndrome
- Basedow's disease
- Basilar Impression Primary
- Basilar Migraine
- Batten Disease
- Bazex-Dupre-Christol Syndrome
- BDSD
- Beaded hair
- Beals Syndrome
- Bechterew disease
- Becker muscular dystrophy
- Becker Nevus Syndrome
- Becker's general myotonia
- Becker's Nevus
- Beckwith-Wiedemann Syndrome
- Bednar's Tumor
- Bedsores
- Bedwetting
- Behavioral Disorders
- Behcet disease
- Behcet's disease
- Behr Syndrome
- Bejel
- Bell's palsy
- Ben Ari Shuper Mimouni Syndrome
- Benign Autosomal Dominant Myopathy
- Benign Congenital Hypotonia
- Benign Eccrine Spiradenoma
- Benign Essential Blepharospasm (BEB)
- Benign Essential Tremor Syndrome
- Benign Familial Hematuria
- Benign Familial Infantile Epilepsy
- Benign familial infantile seizures 3
- Benign familial neonatal seizures
- Benign Familial Neonatal-Infantile Seizures
- Benign hereditary chorea
- Benign Hyperphenylalaninemia
- Benign Lymphoma
- Benign multicystic peritoneal mesothelioma
- Benign Paroxysmal Positional Vertigo
- Benign Prostatic Hyperplasia
- Benign Recurrent Intrahepatic Cholestasis 1
- Benign Recurrent Intrahepatic Cholestasis 2
- Benign rolandic epilepsy
- Benign scapuloperoneal muscular dystrophy with cardiomyopathy
- Benign Tremor
- Bent bone dysplasia syndrome
- Berardinelli-Seip syndrome
- Berger Disease
- Beriberi
- Berman Syndrome
- Bernard-Soulier syndrome
- Bernard-Soulier syndrome type C
- Bernard-Soulier syndrome, type A
- Berylliosis
- Besnier-Boeck-Schaumann Disease
- Best disease
- Bestrophinopathy, autosomal recessive
- Beta ketothiolase deficiency
- Beta mannosidase deficiency
- Beta Mannosidosis
- Beta Thalassemia
- Beta thalassemia, dominant inclusion body type
- Beta-2-microglobulin deficiency
- Beta-D-mannosidosis
- Beta-Galactosidase-1 Deficiency
- Beta-hydroxyisobutyryl coa deacylase deficiency
- Beta-hydroxyisobutyryl-CoA deacylase deficiency
- Beta-Sarcoglycanopathy
- Beta-Thalassemia
- Beta-ureidopropionase deficiency
- Bethlem Myopathy