Source: CURATED ×
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: C0004403
Disease: Autosome Abnormalities
Autosome Abnormalities 		16 0 16 1.00 0 0
CUI: C0034734
Disease: Raynaud Disease
Raynaud Disease 		3 0 2 0.12 0 0
CUI: C0034735
Disease: Raynaud Phenomenon
Raynaud Phenomenon 		3 0 2 0.12 0 0
CUI: C0043346
Disease: Xeroderma Pigmentosum
Xeroderma Pigmentosum 		4 0 2 0.11 0 0
CUI: C0023448
Disease: Lymphoid leukemia
Lymphoid leukemia 		8 0 2 9.1E-02 0 0
CUI: C0042076
Disease: Urologic Neoplasms
Urologic Neoplasms 		8 0 2 9.1E-02 0 0
CUI: C0751571
Disease: Cancer of Urinary Tract
Cancer of Urinary Tract 		8 0 2 9.1E-02 0 0
CUI: C1449861
Disease: Micronuclei, Chromosome-Defective
Micronuclei, Chromosome-Defective 		26 0 3 7.7E-02 0 0
CUI: C1449862
Disease: Micronuclei, Genotoxicant-Induced
Micronuclei, Genotoxicant-Induced 		26 0 3 7.7E-02 0 0
CUI: C0008626
Disease: Congenital chromosomal disease
Congenital chromosomal disease 		1 0 1 6.2E-02 0 0
CUI: C0280141
Disease: Acute Undifferentiated Leukemia
Acute Undifferentiated Leukemia 		1 0 1 6.2E-02 0 0
CUI: C0856823
Disease: Undifferentiated type acute leukemia
Undifferentiated type acute leukemia 		1 0 1 6.2E-02 0 0
CUI: C0969687
Disease: Autosomal Chromosome Disorders
Autosomal Chromosome Disorders 		1 0 1 6.2E-02 0 0
CUI: C1292775
Disease: Acute myeloid leukemia, 11q23 abnormalities
Acute myeloid leukemia, 11q23 abnormalities 		1 0 1 6.2E-02 0 0
CUI: C1853100
Disease: CEREBROOCULOFACIOSKELETAL SYNDROME 4
CEREBROOCULOFACIOSKELETAL SYNDROME 4 		1 0 1 6.2E-02 0 0
CUI: C2673187
Disease: Erythrocytosis, Familial, 4
Erythrocytosis, Familial, 4 		1 0 1 6.2E-02 0 0
CUI: C2752147
Disease: XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C
XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C 		1 0 1 6.2E-02 0 0
CUI: C4014476
Disease: MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 10
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 10 		1 0 1 6.2E-02 0 0
CUI: C4015156
Disease: MICROCEPHALY 12, PRIMARY, AUTOSOMAL RECESSIVE
MICROCEPHALY 12, PRIMARY, AUTOSOMAL RECESSIVE 		1 0 1 6.2E-02 0 0
CUI: C4225278
Disease: GLIOMA SUSCEPTIBILITY 9
GLIOMA SUSCEPTIBILITY 9 		1 0 1 6.2E-02 0 0
CUI: C4225288
Disease: SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION
SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION 		1 0 1 6.2E-02 0 0
CUI: C4551774
Disease: FEINGOLD SYNDROME 1
FEINGOLD SYNDROME 1 		1 0 1 6.2E-02 0 0
CUI: C0032230
Disease: Pleural Rub
Pleural Rub 		2 0 1 5.9E-02 0 0
CUI: C0034642
Disease: Rales
Rales 		2 0 1 5.9E-02 0 0
CUI: C0035234
Disease: Respiratory Sounds
Respiratory Sounds 		2 0 1 5.9E-02 0 0