DisGeNET - a database of gene-disease associations

Short stature, C0349588

N. genes: 190; N. variants: 292

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:	C0020492
Disease:	Hyperostosis

1

2

1

5.3E-03

2

6.8E-03

CUI:	C0020502
Disease:	Hyperparathyroidism

Hyperparathyroidism

1

1

1

5.3E-03

1

3.4E-03

CUI:	C0020517
Disease:	Hypersensitivity

Hypersensitivity

1

0

1

5.3E-03

0

0

CUI:	C0020541
Disease:	Portal Hypertension

Portal Hypertension

1

0

1

5.3E-03

0

0

CUI:	C0020581
Disease:	Hyphema

1

0

1

5.3E-03

0

0

CUI:	C0020635
Disease:	Hypopituitarism

Hypopituitarism

1

1

1

5.3E-03

1

3.4E-03

CUI:	C0023003
Disease:	Langer-Giedion Syndrome

Langer-Giedion Syndrome

1

0

1

5.3E-03

0

0

CUI:	C0023885
Disease:	Liver Abscess

1

1

1

5.3E-03

1

3.4E-03

CUI:	C0024591
Disease:	Malignant hyperpyrexia due to anesthesia

Malignant hyperpyrexia due to anesthesia

1

0

1

5.3E-03

0

0

CUI:	C0025267
Disease:	Multiple Endocrine Neoplasia Type 1

Multiple Endocrine Neoplasia Type 1

1

127

1

5.3E-03

1

2.4E-03

CUI:	C0025268
Disease:	Multiple Endocrine Neoplasia Type 2a

Multiple Endocrine Neoplasia Type 2a

1

31

1

5.3E-03

1

3.1E-03

CUI:	C0025269
Disease:	Multiple Endocrine Neoplasia Type 2b

Multiple Endocrine Neoplasia Type 2b

1

15

1

5.3E-03

1

3.3E-03

CUI:	C0026760
Disease:	Multiple Epiphyseal Dysplasia

Multiple Epiphyseal Dysplasia

1

1

1

5.3E-03

1

3.4E-03

CUI:	C0027080
Disease:	Myoglobinuria

1

1

1

5.3E-03

1

3.4E-03

CUI:	C0027121
Disease:	Myositis

1

1

1

5.3E-03

1

3.4E-03

CUI:	C0027662
Disease:	Multiple Endocrine Neoplasia

Multiple Endocrine Neoplasia

1

0

1

5.3E-03

0

0

CUI:	C0027830
Disease:	neurofibroma

1

0

1

5.3E-03

0

0

CUI:	C0027831
Disease:	Neurofibromatosis 1

Neurofibromatosis 1

1

764

1

5.3E-03

3

2.8E-03

CUI:	C0027888
Disease:	Hereditary Motor and Sensory Neuropathies

Hereditary Motor and Sensory Neuropathies

1

0

1

5.3E-03

0

0

CUI:	C0029443
Disease:	Osteomyelitis

1

1

1

5.3E-03

1

3.4E-03

CUI:	C0030353
Disease:	Papilledema

1

0

1

5.3E-03

0

0

CUI:	C0032897
Disease:	Prader-Willi Syndrome

Prader-Willi Syndrome

1

0

1

5.3E-03

0

0

CUI:	C0033835
Disease:	Pseudopseudohypoparathyroidism

Pseudopseudohypoparathyroidism

1

11

1

5.3E-03

2

6.6E-03

CUI:	C0033999
Disease:	Pterygium

1

1

1

5.3E-03

1

3.4E-03

CUI:	C0037293
Disease:	Skin tag

1

1

1

5.3E-03

1

3.4E-03