Human Phenotype Ontology (HPO)
1824 terms(s) returned
| Term Type: | Record: 451 to 500 of 1824 Records | Page: 10 of 37, First Previous Next Last | Show Records Per Page |
- Mirror image foot polydactyly
- Mirror image hand polydactyly
- Mirror image polydactyly
- Misalignment of incisors
- Misalignment of the pulmonary veins
- Miscarriage
- Misophonia
- Missing ribs
- Mitochondrial depletion
- Mitochondrial encephalopathy
- Mitochondrial hypertrophy
- Mitochondrial inheritance
- Mitochondrial lysine transport defect
- Mitochondrial malic enzyme reduced
- Mitochondrial myopathy
- Mitochondrial propionyl-CoA carboxylase defect
- Mitochondrial respiratory chain defects
- Mitochondrial swelling
- Mitral annular calcification
- Mitral atresia
- Mitral chordae tendinae rupture
- Mitral opening snap
- Mitral regurgitation
- Mitral stenosis
- Mitral valve arcade
- Mitral valve calcification
- Mitral valve leaflet calcification
- Mitral valve prolapse
- Mitten deformity
- Mixed astigmatism
- Mixed cirrhosis
- Mixed demyelinating and axonal polyneuropathy
- Mixed hearing impairment
- Mixed hypo- and hyperpigmentation of the skin
- Mixed respiratory and metabolic acidosis
- Mixed sclerosis of humeral metaphyses
- Mixed total anomalous pulmonary venous connection
- Mizuo phenomenon
- Mobile lump
- Mobitz I atrioventricular block
- Mobitz II atrioventricular block
- Mode of inheritance
- Moderate
- Moderate albuminuria
- Moderate conductive hearing impairment
- Moderate constriction of peripheral visual field
- Moderate expressive language delay
- Moderate generalized osteoporosis
- Moderate global developmental delay
- Moderate hearing impairment
