Human Phenotype Ontology (HPO)
1851 terms(s) returned
| Term Type: | Record: 501 to 550 of 1851 Records | Page: 11 of 38, First Previous Next Last | Show Records Per Page |
- Mixed hearing impairment
- Mixed hypo- and hyperpigmentation of the skin
- Mixed oocyte maturation arrest
- 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
- Moderate hypermetropia
- Moderate intellectual disability
- Moderate intrauterine growth retardation
- Moderate myopia
- Moderate oligozoospermia
- Moderate postnatal growth retardation
- Moderate proteinuria
- Moderate receptive language delay
- Moderate sensorineural hearing impairment
- Moderate to late preterm birth
- Moderately reduced contrast sensitivity
- Moderately reduced left ventricular ejection fraction
- Moderately reduced visual acuity
- Moderately short stature
- Modic type I vertebral endplate changes
- Modic type II vertebral endplate changes
- Modic type III vertebral endplate changes
- Modic type vertebral endplate changes
- Molar incisor malformation
- Molar tooth sign on MRI
- Molarization of premolar
- Molluscoid pseudotumors
- Molybdenum cofactor deficiency
- Mongolian blue spot
- Monilethrix
- Monkey wrench femoral neck
- Monoarticular
- Monocarboxylic aciduria
- Monochromacy
- Monoclonal elevated circulating IgE concentration
- Monoclonal elevation of IgG kappa chain
