Human Disease Ontology
566 terms(s) returned
| Term Type: | Record: 201 to 250 of 566 Records | Page: 5 of 12, First Previous Next Last | Show Records Per Page |
- inability to speak
- inability to swallow
- inability to think clearly
- inactive_catalytic_site
- inactive_ligand_binding_site
- inappropriate ADH syndrome
- inclusion body myopathy and brain white matter abnormalities
- inclusion body myopathy with Paget disease of bone and frontotemporal dementia
- inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1
- inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 2
- inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 3
- inclusion body myositis
- inclusion conjunctivitis
- incomplete X-linked dominant inheritance
- incomplete autosomal dominant inheritance
- incomplete bladder emptying
- incomplete_terminal_codon_variant
- incomplete_transcript_3UTR_variant
- incomplete_transcript_5UTR_variant
- incomplete_transcript_CDS
- incomplete_transcript_coding_splice_variant
- incomplete_transcript_exonic_variant
- incomplete_transcript_intronic_variant
- incomplete_transcript_splice_region_variant
- incomplete_transcript_variant
- incontinence without sensory awareness
- incoordination
- increased appetite
- increased_gene_product_level
- increased_polyadenylation_variant
- increased_transcript_level_variant
- increased_transcript_stability_variant
- increased_transcription_rate_variant
- increased_translational_product_level
- indeterminate leprosy
- indirect transmission
- indolent plasma cell myeloma
- indolent systemic mastocytosis
- infancy electroclinical syndrome
- infant botulism
- infant gynecomastia
- infant symptom
- infant-type hemispheric glioma
- infantile Refsum disease
- infantile cerebellar-retinal degeneration
- infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly
- infantile histiocytoid cardiomyopathy
- infantile hypertrophic cardiomyopathy
- infantile hypophosphatasia
- infantile hypotonia with psychomotor retardation and characteristic facies-3
