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: C4022971
Disease: Hyposerinemia
Hyposerinemia
3 0 3 1.00 0 0
Phosphoserine Aminotransferase Deficiency
2 0 2 0.67 0 0
CUI: C4022973
Disease: Hypoglycinemia
Hypoglycinemia
2 0 2 0.67 0 0
CUI: C4015019
Disease: NEU-LAXOVA SYNDROME 2
NEU-LAXOVA SYNDROME 2
3 0 2 0.50 0 0
3-Phosphoglycerate dehydrogenase deficiency
1 0 1 0.33 0 0
Deficiency of phosphoserine phosphatase
1 0 1 0.33 0 0
Yellow subcutaneous tissue covered by thin, scaly skin
1 0 1 0.33 0 0
CUI: C3552528
Disease: Generalized ichthyosis
Generalized ichthyosis
1 0 1 0.33 0 0
CUI: C1857045
Disease: Abnormality of the philtrum
Abnormality of the philtrum
6 0 2 0.29 0 0
CUI: C0860609
Disease: Inappropriate crying
Inappropriate crying
8 0 2 0.22 0 0
CUI: C4023478
Disease: EEG with focal sharp waves
EEG with focal sharp waves
3 0 1 0.20 0 0
CUI: C0265218
Disease: Neu-Laxova syndrome
Neu-Laxova syndrome
10 0 2 0.18 0 0
CUI: C0266786
Disease: Short cord
Short cord
4 0 1 0.17 0 0
CUI: C0578475
Disease: Cyanotic attack
Cyanotic attack
4 0 1 0.17 0 0
CUI: C0566694
Disease: Small placenta
Small placenta
5 0 1 0.14 0 0
CUI: C0085547
Disease: Phenylketonuria, Maternal
Phenylketonuria, Maternal
6 0 1 0.12 0 0
CUI: C1850327
Disease: Bifid uterus
Bifid uterus
6 0 1 0.12 0 0
CUI: C1861696
Disease: EAR WAX, WET/DRY
EAR WAX, WET/DRY
6 0 1 0.12 0 0
CUI: C0030568
Disease: Parkinson Disease, Postencephalitic
Parkinson Disease, Postencephalitic
7 0 1 0.11 0 0
CUI: C0263978
Disease: Disorder of soft tissue
Disorder of soft tissue
7 0 1 0.11 0 0
CUI: C0270820
Disease: Gelastic Epilepsy
Gelastic Epilepsy
7 0 1 0.11 0 0
CUI: C0338597
Disease: Choroid plexus cyst
Choroid plexus cyst
7 0 1 0.11 0 0
Phosphoglycerate Dehydrogenase Deficiency
7 9 1 0.11 3 0.23
CUI: C0041105
Disease: Trismus
Trismus
18 0 2 0.11 0 0
CUI: C0239783
Disease: Inguinal pain
Inguinal pain
8 0 1 1.0E-01 0 0