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: C0202202
Disease: Protein measurement
Protein measurement
75 0 1 3.2E-03 0 0
CUI: C1839630
Disease: Severe muscular hypotonia
Severe muscular hypotonia
75 0 1 3.2E-03 0 0
CUI: C2132198
Disease: Abnormal blistering of the skin
Abnormal blistering of the skin
75 0 1 3.2E-03 0 0
CUI: C0270853
Disease: Juvenile Myoclonic Epilepsy
Juvenile Myoclonic Epilepsy
74 0 1 3.2E-03 0 0
Hereditary Breast and Ovarian Cancer Syndrome
74 0 1 3.2E-03 0 0
CUI: C1445953
Disease: Poor eye contact
Poor eye contact
73 0 1 3.2E-03 0 0
CUI: C0206696
Disease: Carcinoma, Signet Ring Cell
Carcinoma, Signet Ring Cell
70 0 1 3.2E-03 0 0
CUI: C1866141
Disease: Foot dorsiflexor weakness
Foot dorsiflexor weakness
70 0 1 3.2E-03 0 0
CUI: C0020620
Disease: Hypohidrosis
Hypohidrosis
69 0 1 3.3E-03 0 0
CUI: C0020678
Disease: Hypotrichosis
Hypotrichosis
69 0 1 3.3E-03 0 0
CUI: C1844383
Disease: Recurrent bacterial infection
Recurrent bacterial infection
69 0 1 3.3E-03 0 0
CUI: C0238621
Disease: Aminoaciduria
Aminoaciduria
68 0 1 3.3E-03 0 0
CUI: C0474808
Disease: Follicular neoplasm
Follicular neoplasm
68 0 1 3.3E-03 0 0
CUI: C0522224
Disease: Paralysed
Paralysed
68 0 1 3.3E-03 0 0
CUI: C1963099
Disease: Myelodysplasia, CTCAE
Myelodysplasia, CTCAE
68 0 1 3.3E-03 0 0
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome
67 0 1 3.3E-03 0 0
CUI: C1306214
Disease: ACTH-Secreting Pituitary Adenoma
ACTH-Secreting Pituitary Adenoma
67 0 1 3.3E-03 0 0
CUI: C1850456
Disease: Progressive microcephaly
Progressive microcephaly
67 0 1 3.3E-03 0 0
PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE
67 0 1 3.3E-03 0 0
Familial Nonmedullary Thyroid Cancer
66 0 1 3.3E-03 0 0
CUI: C0027662
Disease: Multiple Endocrine Neoplasia
Multiple Endocrine Neoplasia
65 0 1 3.3E-03 0 0
CUI: C0376705
Disease: Viral Load result
Viral Load result
65 0 1 3.3E-03 0 0
CUI: C0948201
Disease: Alloimmunisation
Alloimmunisation
65 0 1 3.3E-03 0 0
CUI: C0235025
Disease: Peripheral motor neuropathy
Peripheral motor neuropathy
64 0 1 3.3E-03 0 0
CUI: C4021776
Disease: Abnormality of the voice
Abnormality of the voice
64 0 1 3.3E-03 0 0