Mondo Disease Ontology
5944 terms(s) returned
| Term Type: | Record: 2551 to 2600 of 5944 Records | Page: 52 of 119, First Previous Next Last | Show Records Per Page |
- obsolete hypouricemia, renal
- obsolete ichthyosis associated with ocular features
- obsolete idiopathic and/or familial pulmonary arterial hypertension
- obsolete idiopathic inherited hypercalciuria
- obsolete idiopathic interstitial pneumonia
- obsolete idiopathic juvenile osteoporosis
- obsolete idiopathic or cryptogenic familial epilepsy syndrome with identified loci/genes
- obsolete idiopathic pulmonary arterial hypertension
- obsolete idiopathic pulmonary fibrosis
- obsolete idiopathic recurrent and disabling cutaneous herpes
- obsolete immature teratoma of ovary
- obsolete immune deficiency disease
- obsolete immune deficiency with skin involvement
- obsolete immune dysregulation disease with immunodeficiency
- obsolete immune dysregulation with inflammatory bowel disease
- obsolete immune response-regulating cell surface receptor signaling pathway involved in phagocytosis
- obsolete immune suppression
- obsolete immune-mediated acquired neuromuscular junction disease
- obsolete immunodeficiency due to a complement cascade component deficiency
- obsolete immunodeficiency due to a complement regulatory deficiency
- obsolete immunodeficiency due to a genetic complement cascade protein anomaly
- obsolete immunodeficiency due to absence of thymus
- obsolete immunodeficiency predominantly affecting antibody production
- obsolete immunodeficiency syndrome with abnormal pigmentation
- obsolete immunodeficiency syndrome with autoimmunity
- obsolete immunodeficiency with defective leukocyte and lymphocyte function and with response to histamine-1 antagonist
- obsolete immunodeficiency with hyper-IgM
- obsolete immunodeficiency with isotype or light chain deficiencies with normal number of B-cells
- obsolete immunodeficiency with severe reduction in serum IgG and IgA with normal/elevated IgM and normal number of B-cells
- obsolete immunodeficiency without anhidrotic ectodermal dysplasia
- obsolete immunodeficiency, partial combined, with absence of HLA Determinants and beta-2-microglobulin from lymphocytes
- obsolete immunodeficiency-centromeric instability-facial anomalies syndrome
- obsolete immunoglobulin A deficiency
- obsolete immunoglobulin alpha deficiency
- obsolete immunoglobulin switch sequences
- obsolete inborn disorder of gamma-aminobutyric acid metabolism
- obsolete inborn disorder of glycerol metabolism
- obsolete inborn disorder of urea cycle metabolism and ammonia detoxification
- obsolete inborn glycogen metabolism disorder
- obsolete inborn purine-pyrimidine metabolic disorder
- obsolete inborn vitamin B12 deficiency
- obsolete incisors, long upper central
- obsolete inclusion body fibromatosis
- obsolete inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia
- obsolete incontinentia pigmenti achromians
- obsolete increased nucleus size
- obsolete indifference to pain, congenital, autosomal dominant
- obsolete indolalkylamine metabolic process
- obsolete indolent systemic mastocytosis
- obsolete infancy electroclinical syndrome
