Source: CLINVAR ×
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: C0002874
Disease: Aplastic Anemia
Aplastic Anemia 		5 0 1 0.14 0 0
CUI: C0004096
Disease: Asthma
Asthma 		18 0 1 5.0E-02 0 0
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		54 0 1 1.8E-02 0 0
CUI: C0007095
Disease: Carcinoid Tumor
Carcinoid Tumor 		1 0 1 0.33 0 0
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		43 0 1 2.2E-02 0 0
CUI: C0013274
Disease: Patent ductus arteriosus
Patent ductus arteriosus 		23 0 1 4.0E-02 0 0
CUI: C0013336
Disease: Dwarfism
Dwarfism 		9 0 1 9.1E-02 0 0
CUI: C0015625
Disease: Fanconi Anemia
Fanconi Anemia 		15 0 1 5.9E-02 0 0
CUI: C0018681
Disease: Headache
Headache 		19 0 1 4.8E-02 0 0
CUI: C0023449
Disease: Acute lymphocytic leukemia
Acute lymphocytic leukemia 		5 0 1 0.14 0 0
CUI: C0025322
Disease: Premature Menopause
Premature Menopause 		7 0 1 0.11 0 0
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		162 0 1 6.1E-03 0 0
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		336 0 1 3.0E-03 0 0
CUI: C0028754
Disease: Obesity
Obesity 		24 0 1 3.8E-02 0 0
CUI: C0029396
Disease: Heterotopic Ossification
Heterotopic Ossification 		2 0 1 0.25 0 0
CUI: C0035335
Disease: Retinoblastoma
Retinoblastoma 		3 0 1 0.20 0 0
CUI: C0036631
Disease: Seminoma
Seminoma 		1 0 1 0.33 0 0
CUI: C0151786
Disease: Muscle Weakness
Muscle Weakness 		30 0 1 3.1E-02 0 0
CUI: C0152459
Disease: Linear atrophy
Linear atrophy 		2 0 1 0.25 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior 		16 0 1 5.6E-02 0 0
CUI: C0238207
Disease: Ectopic kidney
Ectopic kidney 		2 0 1 0.25 0 0
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma 		4 0 1 0.17 0 0
CUI: C0242363
Disease: Islet Cell Tumor
Islet Cell Tumor 		3 0 1 0.20 0 0
CUI: C0262630
Disease: Reduced concentration span
Reduced concentration span 		2 0 1 0.25 0 0
CUI: C0265529
Disease: Plagiocephaly
Plagiocephaly 		10 0 1 8.3E-02 0 0