Source: CLINVAR ×
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: C0007112
Disease: Adenocarcinoma of prostate
Adenocarcinoma of prostate 		16 96 11 0.28 60 0.17
CUI: C0010606
Disease: Adenoid Cystic Carcinoma
Adenoid Cystic Carcinoma 		11 27 6 0.15 16 4.9E-02
CUI: C0206667
Disease: Adrenal Cortical Adenoma
Adrenal Cortical Adenoma 		2 0 2 5.9E-02 0 0
CUI: C0206686
Disease: Adrenocortical carcinoma
Adrenocortical carcinoma 		7 34 4 0.11 22 6.7E-02
CUI: C1859972
Disease: ADRENOCORTICAL CARCINOMA, HEREDITARY
ADRENOCORTICAL CARCINOMA, HEREDITARY 		1 6 1 2.9E-02 2 6.3E-03
CUI: C1859973
Disease: Adrenocortical Carcinoma, Pediatric
Adrenocortical Carcinoma, Pediatric 		1 2 1 2.9E-02 1 3.2E-03
CUI: C0001768
Disease: Agammaglobulinemia
Agammaglobulinemia 		1 0 1 2.9E-02 0 0
CUI: C3152144
Disease: AGAMMAGLOBULINEMIA 1, AUTOSOMAL RECESSIVE
AGAMMAGLOBULINEMIA 1, AUTOSOMAL RECESSIVE 		2 0 1 2.9E-02 0 0
CUI: C0175754
Disease: Agenesis of corpus callosum
Agenesis of corpus callosum 		23 0 1 1.8E-02 0 0
CUI: C0002170
Disease: Alopecia
Alopecia 		5 5 2 5.4E-02 1 3.1E-03
CUI: C0152207
Disease: Alternating Exotropia
Alternating Exotropia 		1 0 1 2.9E-02 0 0
CUI: C0002418
Disease: Amblyopia
Amblyopia 		17 0 1 2.0E-02 0 0
CUI: C1332262
Disease: Anal canal squamous cell carcinoma
Anal canal squamous cell carcinoma 		1 0 1 2.9E-02 0 0
CUI: C0334579
Disease: Anaplastic astrocytoma
Anaplastic astrocytoma 		1 2 1 2.9E-02 2 6.4E-03
CUI: C0238461
Disease: Anaplastic thyroid carcinoma
Anaplastic thyroid carcinoma 		1 1 1 2.9E-02 1 3.2E-03
CUI: C1260899
Disease: Anemia, Diamond-Blackfan
Anemia, Diamond-Blackfan 		12 0 1 2.2E-02 0 0
CUI: C1840077
Disease: Anteverted nostril
Anteverted nostril 		30 0 1 1.6E-02 0 0
CUI: C2936791
Disease: Antley-Bixler Syndrome, Autosomal Dominant
Antley-Bixler Syndrome, Autosomal Dominant 		1 0 1 2.9E-02 0 0
CUI: C0003466
Disease: Anus, Imperforate
Anus, Imperforate 		9 0 1 2.4E-02 0 0
CUI: C0003467
Disease: Anxiety
Anxiety 		13 0 1 2.2E-02 0 0
CUI: C0001193
Disease: Apert syndrome
Apert syndrome 		1 0 1 2.9E-02 0 0
CUI: C3279222
Disease: Aplasia/Hypoplasia of the cerebellum
Aplasia/Hypoplasia of the cerebellum 		4 0 1 2.7E-02 0 0
CUI: C0264611
Disease: Apraxia of Phonation
Apraxia of Phonation 		10 0 1 2.3E-02 0 0
CUI: C2936786
Disease: Aqueductal Stenosis
Aqueductal Stenosis 		2 2 2 5.9E-02 1 3.2E-03
CUI: C0003803
Disease: Arnold Chiari Malformation
Arnold Chiari Malformation 		3 0 1 2.8E-02 0 0