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: C0079037
Disease: Branchial Clefts-Congenital disorder
Branchial Clefts-Congenital disorder 		1 0 1 0.12 0 0
CUI: C0238293
Disease: Osteomyelosclerosis
Osteomyelosclerosis 		1 0 1 0.12 0 0
CUI: C0264402
Disease: Gas bubble disease
Gas bubble disease 		1 0 1 0.12 0 0
CUI: C0265241
Disease: Franceschetti-Klein syndrome
Franceschetti-Klein syndrome 		1 0 1 0.12 0 0
CUI: C0456877
Disease: High grade T-cell lymphoma
High grade T-cell lymphoma 		1 0 1 0.12 0 0
CUI: C0543612
Disease: Cervical syndrome
Cervical syndrome 		1 0 1 0.12 0 0
CUI: C1332919
Disease: Cervical Mucinous Adenocarcinoma
Cervical Mucinous Adenocarcinoma 		1 0 1 0.12 0 0
CUI: C1854594
Disease: DEAFNESS, AUTOSOMAL DOMINANT 23
DEAFNESS, AUTOSOMAL DOMINANT 23 		1 0 1 0.12 0 0
CUI: C2825742
Disease: Disseminated Juvenile Xanthogranuloma
Disseminated Juvenile Xanthogranuloma 		1 0 1 0.12 0 0
CUI: C3150983
Disease: TREACHER COLLINS SYNDROME 2
TREACHER COLLINS SYNDROME 2 		1 0 1 0.12 0 0
CUI: C4016751
Disease: ANTERIOR SEGMENT ANOMALIES AND CATARACT
ANTERIOR SEGMENT ANOMALIES AND CATARACT 		1 0 1 0.12 0 0
CUI: C4016752
Disease: BRANCHIOOTORENAL SYNDROME WITH CATARACT
BRANCHIOOTORENAL SYNDROME WITH CATARACT 		1 0 1 0.12 0 0
CUI: C4024295
Disease: Hypoplasia of the pharynx
Hypoplasia of the pharynx 		1 0 1 0.12 0 0
CUI: C4025880
Disease: Abnormal parotid gland morphology
Abnormal parotid gland morphology 		1 0 1 0.12 0 0
CUI: C4038750
Disease: RNA polymerase III-related leukodystrophy
RNA polymerase III-related leukodystrophy 		1 0 1 0.12 0 0
CUI: C4225305
Disease: LEUKODYSTROPHY, HYPOMYELINATING, 11
LEUKODYSTROPHY, HYPOMYELINATING, 11 		1 0 1 0.12 0 0
CUI: C0154286
Disease: Iron deficiency anemia secondary to chronic blood loss
Iron deficiency anemia secondary to chronic blood loss 		2 0 1 0.11 0 0
CUI: C0278785
Disease: Recurrent Adult Acute Lymphoblastic Leukemia
Recurrent Adult Acute Lymphoblastic Leukemia 		2 0 1 0.11 0 0
CUI: C0280135
Disease: Ovarian germ cell tumour mixed
Ovarian germ cell tumour mixed 		2 0 1 0.11 0 0
CUI: C0399605
Disease: Commissural lip pit
Commissural lip pit 		2 0 1 0.11 0 0
CUI: C0432562
Disease: Malignant lymphoma of spleen
Malignant lymphoma of spleen 		2 0 1 0.11 0 0
CUI: C1842124
Disease: BRANCHIOOTIC SYNDROME 3 (disorder)
BRANCHIOOTIC SYNDROME 3 (disorder) 		2 0 1 0.11 0 0
CUI: C1850780
Disease: Reduced leukocyte alkaline phosphatase
Reduced leukocyte alkaline phosphatase 		2 0 1 0.11 0 0
CUI: C1855433
Disease: Mandibulofacial dysostosis, Treacher Collins type, autosomal recessive
Mandibulofacial dysostosis, Treacher Collins type, autosomal recessive 		2 0 1 0.11 0 0
CUI: C1862052
Disease: Gustatory lacrimation
Gustatory lacrimation 		2 0 2 0.25 0 0