EPHB2, EPH receptor B2, 2048

N. diseases: 649; N. variants: 19
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
PROSTATE CANCER/BRAIN CANCER SUSCEPTIBILITY (finding)
disease Finding 1 2 0.400 None 0 2
CUI: C0432562
Disease: Malignant lymphoma of spleen
Malignant lymphoma of spleen
disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 2 2 0.010 None 1.000 1 2013 2013
Excessive bleeding from superficial cuts
phenotype Pathologic Function 2 0.100 None 0
CUI: C0398627
Disease: Inherited platelet disorder
Inherited platelet disorder
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 3 0.010 None 1.000 1 2018 2018
CUI: C1446783
Disease: rings tracheal
rings tracheal
disease Anatomical Abnormality 4 0.010 None 1.000 1 2017 2017
CUI: C0266541
Disease: Microphakia
Microphakia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Congenital Abnormality 6 0.010 None 1.000 1 2019 2019
CUI: C0334578
Disease: Papillary ependymoma
Papillary ependymoma
disease Neoplasms Neoplastic Process 6 0.300 None 1.000 1 2015 2015
CUI: C0428419
Disease: Triiodothyronine measurement
Triiodothyronine measurement
phenotype Laboratory Procedure 6 12 0.100 None 1.000 1 1 2019 2019
CUI: C1266045
Disease: Metanephric adenoma
Metanephric adenoma
disease Neoplasms Neoplastic Process 6 2 0.010 None 1.000 1 2018 2018
CUI: C1531553
Disease: Dendritic cell neoplasm
Dendritic cell neoplasm
disease Neoplasms; Hemic and Lymphatic Diseases Neoplastic Process 6 2 0.010 None 1.000 1 2015 2015
CUI: C0221715
Disease: Intestinal carcinoma
Intestinal carcinoma
disease Digestive System Diseases; Neoplasms Neoplastic Process 7 0.010 None 1.000 1 2014 2014
CUI: C1384403
Disease: Cellular Ependymoma
Cellular Ependymoma
disease Neoplasms Neoplastic Process 7 0.300 None 1.000 1 2015 2015
CUI: C1533022
Disease: Histiocytic proliferation
Histiocytic proliferation
disease Disease or Syndrome 7 0.010 None 1.000 1 2019 2019
Acute panmyelosis with myelofibrosis
disease Neoplasms; Hemic and Lymphatic Diseases Neoplastic Process 8 0.010 None 1.000 1 2011 2011
CUI: C1959589
Disease: Angioma, Cavernous
Angioma, Cavernous
disease Neoplasms; Hemic and Lymphatic Diseases; Cardiovascular Diseases Neoplastic Process 9 0.010 None 1.000 1 2018 2018
CUI: C3267126
Disease: Trichodysplasia spinulosa
Trichodysplasia spinulosa
disease Disease or Syndrome 9 0.010 None 1.000 1 2017 2017
CUI: C3672440
Disease: Bile duct hyperplasia
Bile duct hyperplasia
disease Disease or Syndrome 9 0.010 None 1.000 1 2020 2020
CUI: C0263218
Disease: Pyogenic granuloma of skin
Pyogenic granuloma of skin
disease Pathological Conditions, Signs and Symptoms; Neoplasms; Infections; Skin and Connective Tissue Diseases Neoplastic Process 10 3 0.010 None 1.000 1 2019 2019
CUI: C2698750
Disease: Pediatric follicular lymphoma
Pediatric follicular lymphoma
disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 10 0.010 None 1.000 1 2017 2017
CUI: C0272173
Disease: Myelokathexis
Myelokathexis
disease Hemic and Lymphatic Diseases Disease or Syndrome 11 1 0.010 None 1.000 1 2013 2013
SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 2 (disorder)
disease Disease or Syndrome 11 13 0.010 None 1.000 1 2011 2011
CUI: C1860991
Disease: NOONAN SYNDROME 3
NOONAN SYNDROME 3
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases Disease or Syndrome 11 33 0.010 None 1.000 1 2019 2019
CUI: C0205769
Disease: Myxopapillary ependymoma
Myxopapillary ependymoma
disease Neoplasms Neoplastic Process 12 0.300 None 1.000 1 2015 2015
Childhood Chronic Myelogenous Leukemia, BCR-ABL1 Positive
disease Neoplasms; Hemic and Lymphatic Diseases Neoplastic Process 12 1 0.010 None 1.000 1 2011 2011
CUI: C0005866
Disease: Bluetongue infection
Bluetongue infection
disease Infections; Animal Diseases Disease or Syndrome 13 0.010 None 1.000 1 2019 2019