Mondo Disease Ontology
992 terms(s) returned
| Term Type: | Record: 1 to 50 of 992 Records | Page: 1 of 20, First Previous Next Last | Show Records Per Page |
- T cell and NK cell immunodeficiency
- T+ B+ severe combined immunodeficiency
- T-B+ severe combined immunodeficiency
- T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta
- T-B+ severe combined immunodeficiency due to CD45 deficiency
- T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency
- T-B+ severe combined immunodeficiency due to JAK3 deficiency
- T-B+ severe combined immunodeficiency due to gamma chain deficiency
- T-B- severe combined immunodeficiency
- T-cell Subgroups, non-HLA-linked
- T-cell acute lymphoblastic leukemia
- T-cell adult acute lymphocytic leukemia
- T-cell and NK-cell neoplasm
- T-cell childhood acute lymphocytic leukemia
- T-cell childhood lymphoblastic lymphoma
- T-cell immunodeficiency
- T-cell immunodeficiency with epidermodysplasia verruciformis
- T-cell immunodeficiency, congenital alopecia, and nail dystrophy
- T-cell large granular lymphocyte leukemia
- T-cell leukemia
- T-cell lymphopenia, infantile, with or without nail dystrophy, autosomal dominant
- T-cell non-Hodgkin lymphoma
- T-cell prolymphocytic leukemia
- T-cell/histiocyte rich large B cell lymphoma
- T-lymphoblastic lymphoma
- T-substance anomaly
- T2-high asthma
- T2-low asthma
- TARP syndrome
- TCF12-related craniosynostosis
- TCF7L2-related neurodevelopmental disorder
- TCR-alpha-beta-positive T-cell deficiency
- TDP-43 proteinopathy
- TEK-related primary glaucoma
- TELO2-related intellectual disability-neurodevelopmental disorder
- TFEB-rearranged renal cell carcinoma
- TFRC-related combined immunodeficiency
- TH-deficient dopa-responsive dystonia
- TH-deficient infantile parkinsonism and motor delay
- TH-deficient progressive infantile encephalopathy
- THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome
- TMEM165-congenital disorder of glycosylation
- TMEM199-CDG
- TOPORS-related retinopathy
- TORCH syndrome
- TP63-related ectodermal dysplasia spectrum with limb and orofacial malformations
- TPM2-related myopathy
- TPM3-related myopathy
- TPM4-related platelet disorder
- TRAF3 haploinsufficiency
