Pages that link to "Template:Ombox"

The following pages link to Template:Ombox:

Displaying 50 items.

• CNS5:Papillary craniopharyngioma (transclusion) (← links)
• CNS5:Pituicytoma, granular cell tumour of the sellar region, and spindle cell oncocytoma (transclusion) (← links)
• CNS5:Pituitary adenoma / pituitary neuroendocrine tumour (transclusion) (← links)
• CNS5:Pituitary blastoma (transclusion) (← links)
• CNS5:Metastases to the brain and spinal cord parenchyma (transclusion) (← links)
• CNS5:Metastases to the meninges (transclusion) (← links)
• GTS5:Constitutional mismatch repair deficiency (CMMRD) syndrome (MLH1, PMS2, MSH2, MSH6) (transclusion) (← links)
• GTS5:DICER1-related tumour predisposition syndrome (DICER1) (transclusion) (← links)
• GTS5:Neurofibromatosis type 1 (NF1) (transclusion) (← links)
• GTS5:Familial adenomatous polyposis (APC) (transclusion) (← links)
• GTS5:Ataxia-telangiectasia syndrome (ATM) (transclusion) (← links)
• GTS5:Li-Fraumeni syndrome (TP53) (transclusion) (← links)
• GTS5:CHEK2-related hereditary (breast) cancer predisposition syndrome (CHEK2) (transclusion) (← links)
• GTS5:Hereditary gastric and breast cancer syndrome (CDH1, CTNNA1) (transclusion) (← links)
• GTS5:Peutz-Jeghers syndrome (STK11) (transclusion) (← links)
• GTS5:Fanconi anaemia (FANC genes) (transclusion) (← links)
• GTS5:Bloom syndrome (BLM) (transclusion) (← links)
• GTS5:Von Hippel-Lindau syndrome (VHL) (transclusion) (← links)
• GTS5:Klinefelter syndrome (transclusion) (← links)
• GTS5:Turner syndrome (transclusion) (← links)
• GTS5:Down syndrome (transclusion) (← links)
• GTS5:WAGR syndrome (WT1) (transclusion) (← links)
• GTS5:NF2-related schwannomatosis (NF2) (transclusion) (← links)
• GTS5:Multiple endocrine neoplasia type 2 (RET) (transclusion) (← links)
• GTS5:Multiple endocrine neoplasia type 1 (MEN1) (transclusion) (← links)
• GTS5:PTEN hamartoma tumour syndrome (PTEN) (transclusion) (← links)
• GTS5:SDH-deficient tumour syndrome - Hereditary phaeochromocytoma-paraganglioma syndromes (SDHA, SDHB, SDHC, SDHD, SDHAF2) (transclusion) (← links)
• GTS5:Lynch Syndrome (MLH1, PMS2, MSH2, MSH6) (transclusion) (← links)
• GTS5:Hereditary papillary renal carcinoma (MET) (transclusion) (← links)
• GTS5:Juvenile polyposis syndrome (BMPR1A, SMAD4) (transclusion) (← links)
• GTS5:Hereditary neuroblastoma (ALK, PHOX2B) (transclusion) (← links)
• GTS5:Encephalocraniocutaneous lipomatosis (FGFR1) (transclusion) (← links)
• GTS5:Glucagon cell hyperplasia and neoplasia (GCGR) (transclusion) (← links)
• GTS5:McCune-Albright syndrome (GNAS) (transclusion) (← links)
• GTS5:Sturge-Weber syndrome (GNAQ) (transclusion) (← links)
• GTS5:Costello syndrome (HRAS) (transclusion) (← links)
• GTS5:Noonan syndrome (Various genes) (transclusion) (← links)
• GTS5:Schimmelpenning-Feuerstein-Mims (HRAS, KRAS) (transclusion) (← links)
• GTS5:Carney complex (PRKAR1A, PDE8B, PDE11A) (transclusion) (← links)
• GTS5:PROS syndrome (PIK3CA) (transclusion) (← links)
• GTS5:Gastric Adenocarcinoma and Proximal Polyposis of Stomach - GAPPS (APC promoter) (transclusion) (← links)
• GTS5:AXIN2-associated polyposis (AXIN2) (transclusion) (← links)
• GTS5:Serrated polyposis (RNF43) (transclusion) (← links)
• GTS5:WT1 related tumour predisposition syndrome (WT1) (transclusion) (← links)
• GTS5:Hereditary mixed polyposis syndrome (GREM1) (transclusion) (← links)
• GTS5:Naevoid basal cell carcinoma syndrome - Gorlin syndrome (PTCH1, SUFU, GPR161) (transclusion) (← links)
• GTS5:SMO-related Curry-Jones syndrome (SMO) (transclusion) (← links)
• GTS5:ELP1-related medulloblastoma predisposition syndrome(ELP1) (transclusion) (← links)
• GTS5:Osteochondromatosis (EXT1, EXT2) (transclusion) (← links)
• GTS5:Brooke-Spiegler syndrome (CYLD) (transclusion) (← links)