Mondo Disease Ontology
6020 terms(s) returned
| Term Type: | Record: 4351 to 4400 of 6020 Records | Page: 88 of 121, First Previous Next Last | Show Records Per Page |
- combined carcinoid and adenocarcinoma
- combined cervical dystonia
- combined deficiency of factor V and factor VIII
- combined deficiency of factor VII and factor X
- combined deficiency of factors IX and XII, domestic cat
- combined deficiency of factors IX and XII, non-human animal
- combined deficiency of factors VIII, IX, and X, horse
- combined deficiency of factors VIII, IX, and X, non-human animal
- combined dystonia
- combined generalized and focal epilepsy
- combined hamartoma of the retina and retinal pigment epithelium
- combined hepatocellular carcinoma and cholangiocarcinoma
- combined hyperactive dysfunction syndrome of the cranial nerves
- combined immunodeficiency
- combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia
- combined immunodeficiency due to CD3gamma deficiency
- combined immunodeficiency due to CRAC channel dysfunction
- combined immunodeficiency due to CTPS1 deficiency
- combined immunodeficiency due to DOCK8 deficiency
- combined immunodeficiency due to GINS1 deficiency
- combined immunodeficiency due to LRBA deficiency
- combined immunodeficiency due to MALT1 deficiency
- combined immunodeficiency due to ORAI1 deficiency
- combined immunodeficiency due to OX40 deficiency
- combined immunodeficiency due to POLE2 deficiency
- combined immunodeficiency due to RELA haploinsufficiency
- combined immunodeficiency due to STIM1 deficiency
- combined immunodeficiency due to STK4 deficiency
- combined immunodeficiency due to TBX1 deficiency
- combined immunodeficiency due to ZAP70 deficiency
- combined immunodeficiency due to dimerization defective IKAROS mutation
- combined immunodeficiency due to moesin deficiency
- combined immunodeficiency due to partial RAG1 deficiency
- combined immunodeficiency syndrome
- combined immunodeficiency with faciooculoskeletal anomalies
- combined immunodeficiency with low Ig due to BCL10 deficiency
- combined immunodeficiency with skin granulomas
- combined immunodeficiency, X-linked
- combined immunodeficiency-hypogammaglobulinemia-skeletal anomalies syndrome due to IKBKA deficiency
- combined lipase deficiency, LMF1-related, horse
- combined low LDL and fibrinogen
- combined lung carcinoma
- combined malonic and methylmalonic acidemia
- combined osteogenesis imperfecta and Ehlers-Danlos syndrome 1
- combined osteogenesis imperfecta and Ehlers-Danlos syndrome 2
- combined oxidative phosphorylation defect type 11
- combined oxidative phosphorylation defect type 13
- combined oxidative phosphorylation defect type 14
- combined oxidative phosphorylation defect type 15
- combined oxidative phosphorylation defect type 17
