Human Phenotype Ontology (HPO)
1290 terms(s) returned
| Term Type: | Record: 751 to 800 of 1290 Records | Page: 16 of 26, First Previous Next Last | Show Records Per Page |
- 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
- Type II pneumocyte hyperplasia
- Type II pneumocyte hypertrophy
- Type II radial ray deficiency
- Type II transferrin isoform profile
- Type II truncus arteriosus
- Type III atherosclerotic lesion
- Type III radial ray deficiency
- Type III truncus arteriosus
- Type IV atherosclerotic lesion
- Type IV radial ray deficiency
- Type IV truncus arteriosus
- Type V atherosclerotic lesion
- Type VI atherosclerotic lesion
- Typical absence seizure
- Typical absence status epilepticus
- Typical atrial flutter
- Typical perifissural nodule
- Typically de novo
- Typified by age-related disease onset
- Typified by complete penetrance
- Typified by high penetrance
- Typified by highly variable age of onset
- Typified by incomplete penetrance
- Typified by low penetrance
- Typified by moderate penetrance
- Typified by somatic mosaicism
