Experimental Factor Ontology
6962 terms(s) returned
| Term Type: | Record: 1651 to 1700 of 6962 Records | Page: 34 of 140, First Previous Next Last | Show Records Per Page |
- Primary bone dysplasia with defective bone mineralization
- Primary bone dysplasia with micromelia
- Primary bone dysplasia with progressive ossification of skin, skeletal muscle, fascia, tendons and ligaments
- Primary ciliary dyskinesia - retinitis pigmentosa
- Primary congenital hypothyroidism without thyroid developmental anomaly
- Primary dystonia, DYT13 type
- Primary dystonia, DYT21 type
- Primary dystonia, DYT4 type
- Primary dystonia, DYT6 type
- Primary glaucoma
- Primary hemophagocytic lymphohistiocytosis
- Primary hyperaldosteronism
- Primary hypergonadotropic hypogonadism - partial alopecia
- Primary hypomagnesemia with secondary hypocalcemia
- Primary hypothyroidism
- 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 microcephaly
- Primary parathyroids hyperplasia
- Primary tethered chord syndrome
- Prime editing
- Primrose syndrome
- Prinzmetal angina
- Pristionchus pacificus
- Pro-Ala
- Pro-Hyp
- ProP-PD
- ProSAAS
- ProSAAS (human)
- ProSAAS proteolytic cleavage product
- Prochlorococcus marinus
- Prochlorococcus marinus str. MIT 9312
- Prochlorococcus marinus str. MIT 9313
- Prochlorococcus marinus str. MIT 9515
- Prochlorococcus marinus subsp. pastoris str. CCMP1986
- Profiler
- Profound global developmental delay
- Profound hearing impairment
- Profound intellectual disability
- Profound sensorineural hearing impairment
- Profound static encephalopathy
- Progeroid facial appearance
- Progeroid syndrome, Petty type
- Progesterone level
- Progressive cerebellar ataxia
- Progressive cone dystrophy
- Progressive congenital scoliosis
- Progressive distal muscle weakness
