Experimental Factor Ontology
441 terms(s) returned
Term Type: Class | Record: 151 to 200 of 441 Records | Page: 4 of 9, First Previous Next Last | Show Records Per Page |
- nephrotic syndrome 16
- nephrotic syndrome, IIa 26
- nephrotic syndrome, type 22
- nephrotic syndrome, type 4
- nerve plexus neoplasm
- nerve root neoplasm
- nerve sheath neoplasm
- nervous system benign neoplasm
- nervous system disorder, non-human animal
- nervous system neoplasm
- neural tube defect
- neural tube defects, susceptibility to
- neuralgic amyotrophy
- neurenteric cyst
- neurilemmoma of the pleura
- neuritis
- neuritis of upper limb
- neuroacanthocytosis
- neuroaxonal dystrophy
- neuroblastoma, susceptibility to, 1
- neuroblastoma, susceptibility to, 2
- neuroblastoma, susceptibility to, 3
- neurocardiofaciodigital syndrome
- neurocristopathy
- neurocutaneous melanocytosis
- neurocutaneous syndrome
- neurodegeneration and seizures due to copper transport defect
- neurodegeneration with ataxia and late-onset optic atrophy
- neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset
- neurodegeneration with brain iron accumulation
- neurodegeneration with brain iron accumulation 2A
- neurodegeneration with brain iron accumulation 4
- neurodegeneration with brain iron accumulation 5
- neurodegeneration with brain iron accumulation 6
- neurodegeneration with brain iron accumulation 8
- neurodegeneration with developmental delay, early respiratory failure, myoclonic seizures, and brain abnormalities
- neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures
- neurodegeneration, childhood-onset, with ataxia, tremor, optic atrophy, and cognitive decline
- neurodegeneration, childhood-onset, with cerebellar ataxia and cognitive decline
- neurodegeneration, childhood-onset, with hypotonia, respiratory insufficiency, and brain imaging abnormalities
- neurodegeneration, childhood-onset, with multisystem involvement due to mitochondrial dysfunction
- neurodegeneration, childhood-onset, with progressive microcephaly
- neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia
- neurodegeneration, infantile-onset, biotin-responsive
- neurodegenerative syndrome due to cerebral folate transport deficiency
- neurodevelopmental disorder and structural brain anomalies with or without seizures and spasticity
- neurodevelopmental disorder with absent speech and movement and behavioral abnormalities
- neurodevelopmental disorder with alopecia and brain abnormalities
- neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter
- neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies