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: 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
CUI: C0035508
Disease: Rhonchi
Rhonchi 		2 0 1 5.9E-02 0 0
CUI: C0038450
Disease: Stridor
Stridor 		2 0 1 5.9E-02 0 0
CUI: C0043144
Disease: Wheezing
Wheezing 		2 0 1 5.9E-02 0 0
CUI: C0406587
Disease: Wrinkly skin syndrome
Wrinkly skin syndrome 		2 0 1 5.9E-02 0 0
CUI: C0751483
Disease: Familial Retinoblastoma
Familial Retinoblastoma 		2 0 1 5.9E-02 0 0
CUI: C0796068
Disease: Oculodigitoesophagoduodenal syndrome
Oculodigitoesophagoduodenal syndrome 		2 0 1 5.9E-02 0 0
CUI: C1847827
Disease: LIG4 Syndrome
LIG4 Syndrome 		2 0 1 5.9E-02 0 0
CUI: C1854630
Disease: Growth Deficiency and Mental Retardation with Facial Dysmorphism
Growth Deficiency and Mental Retardation with Facial Dysmorphism 		2 0 1 5.9E-02 0 0
CUI: C2826025
Disease: Mixed phenotype acute leukemia
Mixed phenotype acute leukemia 		2 0 1 5.9E-02 0 0