Human Phenotype Ontology (HPO)
33025 terms(s) returned
| Term Type: | Record: 5451 to 5500 of 33025 Records | Page: 110 of 661, First Previous Next Last | Show Records Per Page |
- Central core regions in muscle fibers
- Central corneal dystrophy
- Central cyanosis
- Central diabetes insipidus
- Central diaphragmatic hernia
- Central giant cell lesion of the jaw
- Central heterochromia
- Central hypothyroidism
- Central hypoventilation
- Central nail canal
- Central nervous system axonal spheroid
- Central nervous system cyst
- Central nervous system degeneration
- Central opacification of the cornea
- Central posterior corneal opacity
- Central primitive neuroectodermal tumor
- Central retinal artery occlusion
- Central retinal exudate
- Central retinal vein occlusion
- Central retinal vessel vascular tortuosity
- Central scarring
- Central scotoma
- Central serous chorioretinopathy
- Central sleep apnea
- Central thinning of the outer nuclear layer of the retina
- Central vertebral hypoplasia
- Centrally nucleated skeletal muscle fibers
- Centrilobular
- Centrilobular emphysema
- Centrilobular ground-glass opacification on pulmonary HRCT
- Centrocecal scotoma
- Cephalocele
- Cephalohematoma
- Cerebellar Purkinje layer atrophy
- Cerebellar agenesis
- Cerebellar ataxia associated with quadrupedal gait
- Cerebellar atrophy
- Cerebellar calcifications
- Cerebellar cortical atrophy
- Cerebellar cyst
- Cerebellar dentate nucleus calcification
- Cerebellar dysplasia
- Cerebellar edema
- Cerebellar glioma
- Cerebellar gliosis
- Cerebellar granular layer atrophy
- Cerebellar hemangioblastoma
- Cerebellar hemisphere hypoplasia
- Cerebellar hemorrhage
- Cerebellar hypoplasia
