Mondo Disease Ontology
1854 terms(s) returned
| Term Type: | Record: 351 to 400 of 1854 Records | Page: 8 of 38, First Previous Next Last | Show Records Per Page |
- Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11
- Beemer-Ertbruggen syndrome
- Beemer-Langer syndrome
- Behavior
- Behcet disease
- Behcet syndrome arthropathy
- Behr syndrome
- Behrens Baumann dust syndrome
- Bell's palsy
- Beloniformes
- Bencze syndrome
- Benign prostatic hyperplasia
- Berardinelli-Seip congenital lipodystrophy
- Berk-Tabatznik syndrome
- Bernard-Soulier syndrome
- Bernard-Soulier syndrome, GP9-related, dog
- Bernard-Soulier syndrome, type A2, autosomal dominant
- Beta-cell dysfunction
- Betaarterivirus
- Betaarterivirus americense
- Betacoronavirus
- Betaherpesvirinae
- Betainfluenzavirus
- Betapolyomavirus
- Betapolyomavirus hominis
- Betaproteobacteria
- Bethlem myopathy
- Bethlem myopathy 1A
- Bethlem myopathy 1B
- Bethlem myopathy 1C
- Bethlem myopathy 2
- Bicarbonaturia
- Biceps aplasia
- Biceps hypoplasia
- Bicervical bicornuate uterus and blind hemivagina
- Bicervical bicornuate uterus with patent cervix and vagina
- Bickerstaff brainstem encephalitis
- Biconcave flattened vertebrae
- Biconcave vertebral bodies
- Biemond syndrome type 2
- Bietti crystalline corneoretinal dystrophy
- Bifid distal phalanx of the thumb
- Bifid distal phalanx of toe
- Bifid epiglottis
- Bifid femur
- Bifid first metacarpal
- Bifid humerus
- Bifid nail
- Bifid nasal tip
- Bifid nose
