Source: ALL
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: C0003516
Disease: Aortopulmonary Septal Defect
Aortopulmonary Septal Defect 		1 0 1 1.0E-02 0 0
CUI: C0003910
Disease: Articulation Disorders
Articulation Disorders 		1 0 1 1.0E-02 0 0
CUI: C0007871
Disease: Uterine Cervical Incompetence
Uterine Cervical Incompetence 		1 0 1 1.0E-02 0 0
CUI: C0009761
Disease: Conjunctival Neoplasms
Conjunctival Neoplasms 		1 0 1 1.0E-02 0 0
CUI: C0010334
Disease: Crisscross Heart
Crisscross Heart 		1 0 1 1.0E-02 0 0
CUI: C0027656
Disease: Neoplasms, Connective Tissue
Neoplasms, Connective Tissue 		1 0 1 1.0E-02 0 0
CUI: C0034184
Disease: Pyelocystitis
Pyelocystitis 		1 0 1 1.0E-02 0 0
CUI: C0035290
Disease: Reticulohistiocytic granuloma
Reticulohistiocytic granuloma 		1 0 1 1.0E-02 0 0
CUI: C0037188
Disease: Sinoatrial Block
Sinoatrial Block 		1 0 1 1.0E-02 0 0
CUI: C0151463
Disease: Abscess of breast
Abscess of breast 		1 0 1 1.0E-02 0 0
CUI: C0162504
Disease: Neutrophilic Eccrine Hidradenitis
Neutrophilic Eccrine Hidradenitis 		1 0 1 1.0E-02 0 0
CUI: C0206649
Disease: Neoplasms, Fibroepithelial
Neoplasms, Fibroepithelial 		1 0 1 1.0E-02 0 0
CUI: C0231246
Disease: Failure to gain weight
Failure to gain weight 		1 2 1 1.0E-02 1 0.11
CUI: C0232259
Disease: Mid-systolic murmur
Mid-systolic murmur 		1 0 1 1.0E-02 0 0
CUI: C0235410
Disease: Potassium retention
Potassium retention 		1 0 1 1.0E-02 0 0
CUI: C0238415
Disease: SCLERODERMA, PULMONARY
SCLERODERMA, PULMONARY 		1 0 1 1.0E-02 0 0
CUI: C0238590
Disease: Acrogeria
Acrogeria 		1 0 1 1.0E-02 0 0
CUI: C0240583
Disease: Short upturned nose
Short upturned nose 		1 0 1 1.0E-02 0 0
CUI: C0243057
Disease: Stomatognathic System Abnormalities
Stomatognathic System Abnormalities 		1 0 1 1.0E-02 0 0
CUI: C0262477
Disease: Eye problem
Eye problem 		1 0 1 1.0E-02 0 0
CUI: C0263579
Disease: Pigmented hairy epidermal nevus
Pigmented hairy epidermal nevus 		1 0 1 1.0E-02 0 0
CUI: C0265201
Disease: De Sanctis-Cacchione syndrome
De Sanctis-Cacchione syndrome 		1 0 1 1.0E-02 0 0
CUI: C0265809
Disease: Double outlet left ventricle
Double outlet left ventricle 		1 0 1 1.0E-02 0 0
CUI: C0265843
Disease: Congenital atresia of aortic valve
Congenital atresia of aortic valve 		1 0 1 1.0E-02 0 0
CUI: C0266177
Disease: Megaduodenum
Megaduodenum 		1 0 1 1.0E-02 0 0