DisGeNET - a database of gene-disease associations

Transitional cell carcinoma of bladder, C0279680

N. genes: 26; N. variants: 141

Source: CLINVAR ×

Results per page

Gene

Disease 2

Variant

Source

Semantic type

Disease Class

Type

HPO Term

DO Class

N. genes1

N. genes2

N. of shared genes

Jaccard_g

p-value_g

N. variants1

N. variants2

N. of shared variants

Jaccard_v

p-value_v

Associated Disease

N. genes

N. variants

N. of shared genes

JI_g

p-value_g

N. of shared variants

JI_v

p-value_v

CUI:	C0001080
Disease:	Achondroplasia

1

9

1

3.8E-02

2

1.4E-02

CUI:	C0001418
Disease:	Adenocarcinoma

1

1

1

3.8E-02

1

7.1E-03

CUI:	C0007095
Disease:	Carcinoid Tumor

Carcinoid Tumor

1

1

1

3.8E-02

1

7.1E-03

CUI:	C0007097
Disease:	Carcinoma

1

15

1

3.8E-02

3

2.0E-02

CUI:	C0009451
Disease:	Communicating Hydrocephalus

Communicating Hydrocephalus

1

0

1

3.8E-02

0

0

CUI:	C0030521
Disease:	Parathyroid Neoplasms

Parathyroid Neoplasms

1

2

1

3.8E-02

2

1.4E-02

CUI:	C0033141
Disease:	Cardiomyopathies, Primary

Cardiomyopathies, Primary

1

1

1

3.8E-02

1

7.1E-03

CUI:	C0035934
Disease:	Rubinstein-Taybi Syndrome

Rubinstein-Taybi Syndrome

1

86

1

3.8E-02

1

4.4E-03

CUI:	C0036631
Disease:	Seminoma

1

0

1

3.8E-02

0

0

CUI:	C0152207
Disease:	Alternating Exotropia

Alternating Exotropia

1

0

1

3.8E-02

0

0

CUI:	C0154828
Disease:	Traction detachment of retina

Traction detachment of retina

1

0

1

3.8E-02

0

0

CUI:	C0158763
Disease:	Macrodactylia of fingers

Macrodactylia of fingers

1

1

1

3.8E-02

1

7.1E-03

CUI:	C0158768
Disease:	Macrodactyly of toe

Macrodactyly of toe

1

1

1

3.8E-02

1

7.1E-03

CUI:	C0205770
Disease:	Choroid Plexus Papilloma

Choroid Plexus Papilloma

1

7

1

3.8E-02

2

1.4E-02

CUI:	C0238461
Disease:	Anaplastic thyroid carcinoma

Anaplastic thyroid carcinoma

1

1

1

3.8E-02

1

7.1E-03

CUI:	C0239803
Disease:	Red hair

1

0

1

3.8E-02

0

0

CUI:	C0265552
Disease:	Congenital macrodactylia

Congenital macrodactylia

1

1

1

3.8E-02

1

7.1E-03

CUI:	C0266166
Disease:	Congenital duplication of intestine

Congenital duplication of intestine

1

0

1

3.8E-02

0

0

CUI:	C0271618
Disease:	Delayed female puberty

Delayed female puberty

1

0

1

3.8E-02

0

0

CUI:	C0334579
Disease:	Anaplastic astrocytoma

Anaplastic astrocytoma

1

2

1

3.8E-02

2

1.4E-02

CUI:	C0334586
Disease:	Pleomorphic Xanthoastrocytoma

Pleomorphic Xanthoastrocytoma

1

1

1

3.8E-02

1

7.1E-03

CUI:	C0343114
Disease:	Woolly hair nevus

Woolly hair nevus

1

1

1

3.8E-02

1

7.1E-03

CUI:	C0349661
Disease:	Glial tumor of brain (disorder)

Glial tumor of brain (disorder)

1

0

1

3.8E-02

0

0

CUI:	C0406612
Disease:	Encephalocraniocutaneous lipomatosis

Encephalocraniocutaneous lipomatosis

1

3

1

3.8E-02

1

7.0E-03

CUI:	C0410529
Disease:	Hypochondroplasia (disorder)

Hypochondroplasia (disorder)

1

21

1

3.8E-02

2

1.3E-02