Experimental Factor Ontology
2969 terms(s) returned
| Term Type: | Record: 2051 to 2100 of 2969 Records | Page: 42 of 60, First Previous Next Last | Show Records Per Page |
- neurodevelopmental disorder with relative macrocephaly and with or without cardiac or endocrine anomalies
- neurodevelopmental disorder with seizures and brain abnormalities
- neurodevelopmental disorder with seizures and brain atrophy
- neurodevelopmental disorder with seizures and gingival overgrowth
- neurodevelopmental disorder with seizures and non-epileptic hyperkinetic movements
- neurodevelopmental disorder with seizures and speech and walking impairment
- neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities
- neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities
- neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum
- neurodevelopmental disorder with severe motor impairment and absent language
- 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 speech delay and variable ocular anomalies
- 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 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 measurement
- neurodevelopmental, jaw, eye, and digital syndrome
- neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities
- neuroectodermal melanolysosomal disease
- neuroectodermal-endocrine syndrome
- neuroendocrine carcinoma
- neuroendocrine cell
- neuroendocrine cell hyperplasia of infancy
- neuroendocrine convertase 1
- neuroendocrine convertase 1 (human)
- neuroendocrine convertase 1 measurement
- neuroendocrine convertase 2
- neuroendocrine convertase 2 (human)
- neuroendocrine disorder
- neuroendocrine gland
- neuroendocrine neoplasm
- neuroendocrine protein 7B2
- neuroendocrine protein 7B2 (human)
- neuroendocrine protein 7B2, signal peptide removed form
- neuroendocrine secretory protein 55 isoform Nesp55 (human)
