Experimental Factor Ontology
136 terms(s) returned
Term Type: | Record: 101 to 136 of 136 Records | Page: 3 of 3, First Previous Next Last | Show Records Per Page |
- Primary immunodeficiency due to a defect in innate immunity
- Primary interstitial lung disease specific to childhood due to pulmonary surfactant protein anomalies
- Primary intraosseous vascular malformation
- Primary lateral sclerosis
- Primary parathyroids hyperplasia
- Primary tethered chord syndrome
- Progeroid syndrome, Petty type
- Progressive cone dystrophy
- Progressive epilepsy - intellectual disability, Finnish type
- Progressive external ophthalmoplegia - myopathy - emaciation
- Progressive myoclonic epilepsy
- Progressive sensorineural hearing loss - hypertrophic cardiomyopathy
- Progressive supranuclear palsy - corticobasal syndrome
- Progressive supranuclear palsy - parkinsonism
- Progressive supranuclear palsy - progressive non fluent aphasia
- Progressive supranuclear palsy - pure akinesia with gait freezing
- Progéria - short stature - pigmented nevi
- Prominent glabella - microcephaly - hypogenitalism
- Properdin deficiency
- Proteasome disability syndrome
- Proximal 16p11.2 microduplication syndrome
- Proximal myotonic myopathy
- Proximal spinal muscular atrophy type 2
- Proximal spinal muscular atrophy type 3
- Proximal spinal muscular atrophy type 4
- Proximal tubulopathy - diabetes mellitus - cerebellar ataxia
- Pseudoxanthoma elasticum
- Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency
- Pterygium colli - intellectual disability - digital anomalies
- Pterygium of the conjunctiva, familial form
- Ptosis - strabismus - ectopic pupils
- Ptosis - syndactyly - learning difficulties
- Ptosis - upper ocular movement limitation - absence of lacrimal punctum
- Ptosis - vocal cord paralysis
- Pulmonary capillary hemangiomatosis
- Pyogenic arthritis - pyoderma gangrenosum - acne