Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Malformation of the hepatic ductal plate
1 0 1 1.00 0 0
CUI: C0013608
Disease: Edema, Cardiac
Edema, Cardiac
3 0 1 0.33 0 0
CUI: C1504405
Disease: Pyramidal Tract Dysfunction
Pyramidal Tract Dysfunction
3 0 1 0.33 0 0
SPASTIC PARAPLEGIA 45, AUTOSOMAL RECESSIVE
3 0 1 0.33 0 0
Broad distal phalanges of all fingers
3 0 1 0.33 0 0
Short rib-polydactyly syndrome, Beemer type
6 0 1 0.17 0 0
CUI: C0270720
Disease: Hydrocephalus Ex-Vacuo
Hydrocephalus Ex-Vacuo
7 0 1 0.14 0 0
CUI: C0477432
Disease: Post-Traumatic Hydrocephalus
Post-Traumatic Hydrocephalus
7 0 1 0.14 0 0
CUI: C2936718
Disease: Fetal Cerebral Ventriculomegaly
Fetal Cerebral Ventriculomegaly
7 0 1 0.14 0 0
CUI: C3711371
Disease: Spastic Paraplegia Type 4
Spastic Paraplegia Type 4
7 0 1 0.14 0 0
CUI: C0423823
Disease: Thin nails
Thin nails
10 0 1 1.0E-01 0 0
CUI: C0432235
Disease: CRANIOECTODERMAL DYSPLASIA 1
CRANIOECTODERMAL DYSPLASIA 1
10 0 1 1.0E-01 0 0
CUI: C1835171
Disease: Hypomagnesemia 2, renal
Hypomagnesemia 2, renal
10 0 1 1.0E-01 0 0
Spastic paraplegia 4, autosomal dominant
10 0 1 1.0E-01 0 0
CUI: C0423808
Disease: Brachyonychia
Brachyonychia
11 0 1 9.1E-02 0 0
CUI: C1857527
Disease: Flattened epiphysis
Flattened epiphysis
11 0 1 9.1E-02 0 0
CUI: C1865038
Disease: Broad toe
Broad toe
11 0 1 9.1E-02 0 0
CUI: C4021787
Disease: Abnormal diaphysis morphology
Abnormal diaphysis morphology
11 0 1 9.1E-02 0 0
CUI: C4551571
Disease: Cranioectodermal dysplasia
Cranioectodermal dysplasia
11 0 1 9.1E-02 0 0
CUI: C2699746
Disease: Syndactyly, type 2
Syndactyly, type 2
15 0 1 6.7E-02 0 0
CUI: C1832119
Disease: Fibular hypoplasia
Fibular hypoplasia
16 0 1 6.2E-02 0 0
CUI: C2931150
Disease: Synostotic Anterior Plagiocephaly
Synostotic Anterior Plagiocephaly
16 0 1 6.2E-02 0 0
CUI: C4021664
Disease: Abnormality of the abdominal wall
Abnormality of the abdominal wall
17 0 1 5.9E-02 0 0
CUI: C0549423
Disease: Obstructive Hydrocephalus
Obstructive Hydrocephalus
18 0 1 5.6E-02 0 0
CUI: C4551902
Disease: Craniosynostosis, Type 1
Craniosynostosis, Type 1
18 0 1 5.6E-02 0 0