Human Phenotype Ontology (HPO)
1824 terms(s) returned
| Term Type: | Record: 651 to 700 of 1824 Records | Page: 14 of 37, First Previous Next Last | Show Records Per Page |
- Multiple lentigines
- Multiple lineage myelodysplasia
- Multiple lipomas
- Multiple long-bone exostoses
- Multiple meningiomas
- Multiple mitochondrial DNA deletions
- Multiple mononeuropathy
- Multiple mucosal neuromas
- Multiple muscular ventricular septal defects
- Multiple myeloma
- Multiple non-erupting secondary teeth
- Multiple palmar creases
- Multiple pancreatic beta-cell adenomas
- Multiple plantar creases
- Multiple prenatal fractures
- Multiple pterygia
- Multiple pulmonary cysts
- Multiple pulmonary interstitial hyalinized nodules
- Multiple renal cysts
- Multiple rib fractures
- Multiple rows of eyelashes
- Multiple skeletal anomalies
- Multiple small bowel atresias
- Multiple small medullary renal cysts
- Multiple small vertebral fractures
- Multiple suture craniosynostosis
- Multiple trichilemmomata
- Multiple unerupted teeth
- Multiple-finger involvement
- Mus musculus protein
- Muscle abnormality related to mitochondrial dysfunction
- Muscle arteriovenous malformation
- Muscle eosinophilia
- Muscle extensor surface location
- Muscle fiber actin filament accumulation
- Muscle fiber atrophy
- Muscle fiber calsequestrin 1-containing inclusion bodies
- Muscle fiber cytoplasmatic inclusion bodies
- Muscle fiber fuchsinophilic inclusion bodies
- Muscle fiber granulofilamentous inclusion bodies
- Muscle fiber hyaline bodies
- Muscle fiber inclusion bodies
- Muscle fiber intracytoplasmic reducing inclusion bodies
- Muscle fiber intranuclear inclusion bodies
- Muscle fiber necrosis
- Muscle fiber polyglucosan inclusion bodies
- Muscle fiber splitting
- Muscle fiber tubular inclusions
- Muscle fiber tubuloreticular inclusions
- Muscle fibrillation
