Experimental Factor Ontology
606 terms(s) returned
Term Type: | Record: 201 to 250 of 606 Records | Page: 5 of 13, First Previous Next Last | Show Records Per Page |
- inborn organic aciduria
- inborn serine deficiency
- inborn vitamin B12 deficiency
- inclusion body myopathy and brain white matter abnormalities
- inclusion body myopathy with Paget disease of bone and frontotemporal dementia
- inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1
- incontinentia pigmenti
- indeterminate sex and/or pseudohermaphroditism
- indifference to pain, congenital, autosomal dominant
- indolent B-cell non-Hodgkin lymphoma
- indolent primary cutaneous B-cell lymphoma
- indolent primary cutaneous T-cell lymphoma
- infancy electroclinical syndrome
- infant botulism
- infant-type hemispheric glioma
- infantile Krabbe disease
- infantile axonal neuropathy
- infantile bilateral striatal necrosis
- infantile cataract, skin abnormalities, glutamate excess, and impaired intellectual development
- infantile cerebellar-retinal degeneration
- infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly
- infantile convulsions and choreoathetosis
- infantile diarrhea
- infantile epilepsy syndrome
- infantile epileptic-dyskinetic encephalopathy
- infantile glycine encephalopathy
- infantile hemangioma of rare localization
- infantile hypertrophic cardiomyopathy due to MRPL44 deficiency
- infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome
- infantile liver failure
- infantile liver failure syndrome 1
- infantile liver failure syndrome 2
- infantile myofibromatosis
- infantile neuronal ceroid lipofuscinosis
- infantile osteopetrosis with neuroaxonal dysplasia
- infantile spams-psychomotor retardation-progressive brain atrophy-basal ganglia disease syndrome
- infantile spasms-broad thumbs syndrome
- infantile systemic hyalinosis
- infantile-onset X-linked spinal muscular atrophy
- infantile-onset ascending hereditary spastic paralysis
- infantile-onset autosomal recessive nonprogressive cerebellar ataxia
- infantile-onset epilepsy
- infantile-onset generalized dyskinesia with orofacial involvement
- infantile-onset mesial temporal lobe epilepsy with severe cognitive regression
- infantile-onset periodic fever-panniculitis-dermatosis syndrome
- infection due to clostridium perfringens
- infection-related hemolytic uremic syndrome
- infectious anterior uveitis
- infectious disease characteristic
- infectious disease, non-human animal