Human Disease Ontology
607 terms(s) returned
| Term Type: | Record: 201 to 250 of 607 Records | Page: 5 of 13, First Previous Next Last | Show Records Per Page |
- immunodeficiency 94
- immunodeficiency 95
- immunodeficiency 96
- immunodeficiency 97
- immunodeficiency 98
- immunodeficiency 99
- immunodeficiency with hyper IgM type 3
- immunodeficiency with hyper IgM type 5
- immunodeficiency with hyper-IgM type 2
- immunodeficiency with hyper-IgM type 4
- immunodeficiency-centromeric instability-facial anomalies syndrome
- immunodeficiency-centromeric instability-facial anomalies syndrome 1
- immunodeficiency-centromeric instability-facial anomalies syndrome 2
- immunodeficiency-centromeric instability-facial anomalies syndrome 3
- immunodeficiency-centromeric instability-facial anomalies syndrome 4
- immunoglobulin alpha deficiency
- immunoglobulin beta deficiency
- immunoglobulin heavy chain amyloidosis
- immunoglobulin heavy-and-light chain
- immunoglobulin light chain amyloidosis
- impaired coordination
- impaired gag reflex
- imperforate anus
- impetigo
- impetigo herpetiformis
- impotence
- impulse control disorder
- in situ carcinoma
- in_subset
- inability to comprehend speech
- inability to concentrate
- inability to feed
- inability to form words
- inability to lie flat
- 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
