Mondo Disease Ontology
5261 terms(s) returned
| Term Type: | Record: 1251 to 1300 of 5261 Records | Page: 26 of 106, First Previous Next Last | Show Records Per Page |
- Pyuria
- p-block element atom
- p-block molecular entity
- pachydermodactyly, familial
- pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures
- pachygyria-intellectual disability-epilepsy syndrome
- pachyonychia congenita
- pachyonychia congenita 1
- pachyonychia congenita 2
- pachyonychia congenita 3
- pachyonychia congenita 4
- pacman dysplasia
- paget disease of bone 4
- pagon stephan syndrome
- pain agnosia
- pain management
- painful legs and moving toes syndrome
- painful orbital and systemic neurofibromas-marfanoid habitus syndrome
- pair of dorsal aortae
- pair of lungs
- pair of nares
- paired limb/fin
- paired limb/fin bud
- paired limb/fin bud mesenchyme
- paired limb/fin cartilage
- paired limb/fin field
- paired limb/fin segment
- paired limb/fin skeleton
- paired venous dural sinus
- palant cleft palate syndrome
- palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome
- palatal muscle
- palatal neoplasm
- palatal part of dermatocranium
- palatal taste bud
- palatal tooth
- palate bone
- palatine aponeurosis
- palatine tonsil
- palatine uvula
- palatoquadrate arch
- palindromic rheumatism
- pallium
- palmar fibromatosis
- palmar part of manus
- palmar/plantar part of autopod
- palmar/plantar sweat gland
- palmaris longus muscle, absence of
- palmer pagon syndrome
- palmitoyltransferase activity
