Mondo Disease Ontology
2360 terms(s) returned
| Term Type: | Record: 1701 to 1750 of 2360 Records | Page: 35 of 48, First Previous Next Last | Show Records Per Page |
- neurodevelopmental disorder with severe motor impairment, absent language, cerebral hypomyelination, and brain atrophy
- neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties
- neurodevelopmental disorder with spastic quadriplegia and brain abnormalities with or without seizures
- neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies
- neurodevelopmental disorder with spasticity and poor growth
- neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia
- neurodevelopmental disorder with spasticity, seizures, and brain abnormalities
- neurodevelopmental disorder with spasticity, thin corpus callosum, and decreased brain white matter
- neurodevelopmental disorder with speech delay and behavioral abnormalities
- neurodevelopmental disorder with speech delay and variable ocular anomalies
- neurodevelopmental disorder with speech delay, movement abnormalities, and seizures
- neurodevelopmental disorder with speech impairment and dysmorphic facies
- neurodevelopmental disorder with speech impairment and with or without seizures
- neurodevelopmental disorder with speech or visual impairment and brain hypomyelination
- neurodevelopmental disorder with structural brain abnormalities and craniofacial abnormalities
- neurodevelopmental disorder with structural brain anomalies and dysmorphic facies
- neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language
- neurodevelopmental disorder with variable familial hypercholanemia
- neurodevelopmental disorder with visual defects and brain anomalies
- neurodevelopmental disorder with white matter abnormalities and gait disturbance
- neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures
- neurodevelopmental disorder, nonprogressive, with spasticity and transient opisthotonus
- neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-hip dysplasia syndrome
- neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-hip dysplasia syndrome due to 9q21 microdeletion
- neurodevelopmental, jaw, eye, and digital syndrome
- neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities
- neuroectodermal melanolysosomal disease
- neuroectodermal-endocrine syndrome
- neuroendocrine carcinoma
- neuroendocrine carcinoma of salivary glands, sensorineural hearing loss, and enamel hypoplasia
- neuroendocrine cell
- neuroendocrine cell hyperplasia of infancy
- neuroendocrine cell of epithelium of lobar bronchus
- neuroendocrine disorder
- neuroendocrine gland
- neuroendocrine neoplasm
- neuroendocrine system
- neuroendocrine tumor of the anal canal
- neuroendocrine tumor of the appendix, well differentiated, low or intermediate grade
- neuroendocrine tumor of the colon, well differentiated, low or intermediate grade tumor
- neuroepithelial neoplasm
- neuroepithelioma
- neurofaciodigitorenal syndrome
- neurofacioskeletal syndrome with or without renal agenesis
- neuroferritinopathy
- neurofibroma
- neurofibroma of gallbladder
- neurofibroma of spinal cord
- neurofibroma of the esophagus
- neurofibroma of the heart
