Mondo Disease Ontology
1603 terms(s) returned
Term Type: | Record: 451 to 500 of 1603 Records | Page: 10 of 33, First Previous Next Last | Show Records Per Page |
- Fusobacteriaceae infectious disease
- Fusobacteriales
- Fusobacteriati
- Fusobacteriia
- Fusobacteriota
- Fusobacterium
- Fusobacterium infectious disease
- fabids
- face
- face skin environment
- facial abnormalities, kyphoscoliosis, and intellectual disability
- facial arteriovenous malformation
- facial artery
- facial bone
- facial cleft
- facial clefting corpus callosum agenesis
- facial dermatosis
- facial dermoid cyst
- facial digital syndrome, cattle
- facial digital syndrome, non-human animal
- facial diplegia with paresthesias
- facial dysmorphism, cleft palate, hearing loss, and camptodactyly
- facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome
- facial dysmorphism, selective tooth agenesis, and choroid calcification
- facial dysmorphism-anorexia-cachexia-eye and skin anomalies syndrome
- facial dysmorphism-immunodeficiency-livedo-short stature syndrome
- facial dysmorphism-lens dislocation-anterior segment abnormalities-spontaneous filtering blebs syndrome
- facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome
- facial dysmorphism-shawl scrotum-joint laxity syndrome
- facial dysplasia syndrome, cattle
- facial dysplasia syndrome, non-human animal
- facial eczema, cattle
- facial eczema, non-human animal
- facial eczema, sheep
- facial hemiatrophy
- facial lymph node
- facial lymphatic vessel
- facial mesenchyme
- facial muscle
- facial nerve
- facial nerve canal
- facial nerve disorder
- facial nerve neoplasm
- facial nerve root
- facial neuralgia
- facial nucleus
- facial onset sensory and motor neuronopathy
- facial palsy, congenital, with ptosis and velopharyngeal dysfunction
- facial paralysis
- facial paresis, hereditary congenital, 1