Experimental Factor Ontology
606 terms(s) returned
| Term Type: | Record: 1 to 50 of 606 Records | Page: 1 of 13, First Previous Next Last | Show Records Per Page |
- T lymphoblastic leukemia/lymphoma
- 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 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-lymphoblastic lymphoma
- T-substance anomaly
- T2-high asthma
- TARP syndrome
- TCF12-related craniosynostosis
- TCF7L2-related neurodevelopmental disorder
- TCR-alpha-beta-positive T-cell deficiency
- TFAP2B-related congenital heart disease spectrum disorder
- TFRC-related combined immunodeficiency
- TH-deficient dopa-responsive dystonia
- THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome
- TMEM165-congenital disorder of glycosylation
- TMEM199-CDG
- TNF receptor 1-associated periodic fever syndrome
- TNFRSF9-related immunodeficiency
- TNNT2-related cardiomyopathy
- TOPORS-related retinopathy
- TOR1AIP1-related myopathy
- TOR1AIP1-related nuclear envelopathy
- TP63-related ectodermal dysplasia spectrum with limb and orofacial malformations
- TPM2-related myopathy
- TPM3-related myopathy
- TRAF3 haploinsufficiency
- TREX1-related type 1 interferonopathy
- TRIP11-related skeletal dysplasia
- TRPV4-related bone disorder
- TSEN2-related neurodevelopmental disorder with or without thrombotic microangiopathy
- TSH producing pituitary tumor
