Human Phenotype Ontology (HPO)
33025 terms(s) returned
| Term Type: | Record: 19751 to 19800 of 33025 Records | Page: 396 of 661, First Previous Next Last | Show Records Per Page |
- Tubulointerstitial mycobacterial infiltration
- Tubulointerstitial nephritis
- Tubulointerstitial viral infiltration
- Tubulonodular pericallosal lipoma
- Tufted angioma
- Tufted hairs
- Tumor signet ring cell
- Turricephaly
- Twelfth rib hypoplasia
- Twin pregnancy
- Twin-to-twin transfusion
- Twisted gallbladder pedicle
- Two carpal ossification centers present at birth
- Two-raphe bicuspid aortic valve
- Tympanic membrane bulging
- Tympanic membrane bulla
- Tympanic membrane hypermobility
- Tympanosclerosis
- Type 1 and type 2 muscle fiber minicore regions
- Type 1 collagen overmodification
- Type 1 congenital pulmonary airway malformation
- Type 1 fibers relatively smaller than type 2 fibers
- Type 1 muscle fiber atrophy
- Type 1 muscle fiber predominance
- Type 1 schizencephaly
- Type 2 congenital pulmonary airway malformation
- Type 2 muscle fiber atrophy
- Type 2 muscle fiber predominance
- Type 2 schizencephaly
- Type 3 congenital pulmonary airway malformation
- Type 3 schizencephaly
- Type A brachydactyly
- Type A1 brachydactyly
- Type A2 brachydactyly
- Type A4 brachydactyly
- Type A5 brachydactyly
- Type B brachydactyly
- Type C brachydactyly
- Type D brachydactyly
- Type E brachydactyly
- Type I atherosclerotic lesion
- Type I cryptotia
- Type I diabetes mellitus
- Type I radial ray deficiency
- Type I transferrin isoform profile
- Type I truncus arteriosus
- Type II atherosclerotic lesion
- Type II cryptotia
- Type II diabetes mellitus
- Type II lissencephaly
