Experimental Factor Ontology
3015 terms(s) returned
| Term Type: | Record: 1901 to 1950 of 3015 Records | Page: 39 of 61, First Previous Next Last | Show Records Per Page |
- neurocalcin-delta, initiator methionine removed form (human)
- neurocan core protein
- neurocan core protein (human)
- neurocan core protein, signal peptide removed form
- neurocan core protein, signal peptide removed form (human)
- neurocardiofaciodigital syndrome
- neurocranial trabecula
- 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 2B
- neurodegeneration with brain iron accumulation 4
- neurodegeneration with brain iron accumulation 5
- neurodegeneration with brain iron accumulation 6
- neurodegeneration with brain iron accumulation 7
- neurodegeneration with brain iron accumulation 8
- neurodegeneration with brain iron accumulation 9
- 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 cerebellar atrophy
- 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
- neurodegeneration, infantile-onset, with optic atrophy and brain abnormalities
- neurodegenerative disease
- neurodegenerative disorder, X-linked, female-restricted, with parkinsonism and cognitive impairment
- neurodegenerative syndrome due to cerebral folate transport deficiency
- neurodermatitis
- neurodevelopmental disorder
- neurodevelopmental disorder and structural brain anomalies with or without seizures and spasticity
- neurodevelopmental disorder plus optic atrophy
- neurodevelopmental disorder with absent language and variable seizures
- neurodevelopmental disorder with absent speech and movement and behavioral abnormalities
- neurodevelopmental disorder with achalasia, polyneuropathy, and alacrima
- neurodevelopmental disorder with alopecia and brain abnormalities
- neurodevelopmental disorder with ataxia and brain abnormalities
- neurodevelopmental disorder with ataxia, hypotonia, and microcephaly
- neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter
- neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia
- neurodevelopmental disorder with behavioral, ear, and skeletal abnormalities
- neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies
