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: C0025268
Disease: Multiple Endocrine Neoplasia Type 2a
Multiple Endocrine Neoplasia Type 2a 		69 44 14 7.1E-02 8 0.15
CUI: C0031511
Disease: Pheochromocytoma
Pheochromocytoma 		344 186 32 7.0E-02 7 3.5E-02
CUI: C4551683
Disease: Adrenal Gland Pheochromocytoma
Adrenal Gland Pheochromocytoma 		416 50 33 6.3E-02 7 0.11
CUI: C0238462
Disease: Medullary carcinoma of thyroid
Medullary carcinoma of thyroid 		330 71 42 9.8E-02 6 7.1E-02
CUI: C1833921
Disease: Familial medullary thyroid carcinoma
Familial medullary thyroid carcinoma 		56 45 11 5.9E-02 5 8.5E-02
CUI: C0025267
Disease: Multiple Endocrine Neoplasia Type 1
Multiple Endocrine Neoplasia Type 1 		145 156 18 6.7E-02 4 2.3E-02
CUI: C0025269
Disease: Multiple Endocrine Neoplasia Type 2b
Multiple Endocrine Neoplasia Type 2b 		13 21 4 2.6E-02 4 0.11
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary 		88 6387 11 5.0E-02 4 6.2E-04
CUI: C1970712
Disease: Multiple Endocrine Neoplasia, Type IV
Multiple Endocrine Neoplasia, Type IV 		13 23 3 2.0E-02 4 0.11
CUI: C4048306
Disease: Multiple endocrine neoplasia Type 2
Multiple endocrine neoplasia Type 2 		56 38 12 6.5E-02 4 7.5E-02
CUI: C0010308
Disease: Congenital Hypothyroidism
Congenital Hypothyroidism 		94 48 17 7.8E-02 3 4.7E-02
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis 		6385 327 100 1.6E-02 3 8.7E-03
CUI: C0027651
Disease: Neoplasms
Neoplasms 		10161 1644 118 1.2E-02 3 1.8E-03
CUI: C0342190
Disease: C-cell hyperplasia of thyroid
C-cell hyperplasia of thyroid 		35 16 16 9.9E-02 3 9.4E-02
CUI: C3888239
Disease: HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 1
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 1 		12 52 1 6.5E-03 3 4.4E-02
CUI: C0018213
Disease: Graves Disease
Graves Disease 		585 352 53 7.9E-02 2 5.4E-03
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma 		1348 204 80 5.7E-02 2 9.0E-03
CUI: C0271829
Disease: Pendred's syndrome
Pendred's syndrome 		35 142 13 7.9E-02 2 1.3E-02
CUI: C3538946
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 4, WITH ENLARGED VESTIBULAR AQUEDUCT
DEAFNESS, AUTOSOMAL RECESSIVE 4, WITH ENLARGED VESTIBULAR AQUEDUCT 		10 81 3 2.0E-02 2 2.0E-02
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality 		1098 73 47 3.9E-02 1 1.1E-02
CUI: C0002170
Disease: Alopecia
Alopecia 		491 375 17 2.8E-02 1 2.5E-03
CUI: C0002171
Disease: Alopecia Areata
Alopecia Areata 		114 54 6 2.4E-02 1 1.4E-02
CUI: C0003864
Disease: Arthritis
Arthritis 		1072 69 37 3.1E-02 1 1.1E-02
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		2723 2387 75 2.7E-02 1 4.2E-04
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		1758 428 48 2.6E-02 1 2.2E-03