Source: ALL
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: C4023400
Disease: Generalized hypopigmentation of hair
Generalized hypopigmentation of hair 		6 0 5 0.12 0 0
CUI: C3839753
Disease: Abnormality of nail of toe
Abnormality of nail of toe 		26 0 7 0.12 0 0
CUI: C1855710
Disease: Bone marrow hypocellularity
Bone marrow hypocellularity 		64 0 11 0.12 0 0
CUI: C1148551
Disease: X-Linked Dyskeratosis Congenita
X-Linked Dyskeratosis Congenita 		17 0 6 0.12 0 0
CUI: C2132198
Disease: Abnormal blistering of the skin
Abnormal blistering of the skin 		75 0 12 0.12 0 0
CUI: C0152009
Disease: White blood cell abnormality
White blood cell abnormality 		8 0 5 0.12 0 0
CUI: C0040588
Disease: Tracheoesophageal Fistula
Tracheoesophageal Fistula 		80 0 12 0.11 0 0
CUI: C0432235
Disease: CRANIOECTODERMAL DYSPLASIA 1
CRANIOECTODERMAL DYSPLASIA 1 		10 0 5 0.11 0 0
CUI: C0221260
Disease: Dystrophia unguium
Dystrophia unguium 		81 0 12 0.11 0 0
CUI: C0240310
Disease: Hypoplasia of the maxilla
Hypoplasia of the maxilla 		113 0 15 0.11 0 0
CUI: C2986691
Disease: Inherited bone marrow failure syndrome
Inherited bone marrow failure syndrome 		11 0 5 0.11 0 0
CUI: C4551571
Disease: Cranioectodermal dysplasia
Cranioectodermal dysplasia 		11 0 5 0.11 0 0
CUI: C0270685
Disease: Cerebral calcification
Cerebral calcification 		103 0 14 0.11 0 0
CUI: C0027543
Disease: Avascular necrosis of bone
Avascular necrosis of bone 		73 0 11 0.11 0 0
CUI: C0427515
Disease: Neutrophil abnormality
Neutrophil abnormality 		74 0 11 0.11 0 0
CUI: C0240340
Disease: Microdontia (disorder)
Microdontia (disorder) 		109 6 14 0.10 1 6.7E-02
CUI: C1855925
Disease: Hyperopia, High
Hyperopia, High 		47 0 8 0.10 0 0
CUI: C1851970
Disease: DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT 		4 0 4 1.0E-01 0 0
CUI: C4021631
Disease: Abnormal tracheobronchial morphology
Abnormal tracheobronchial morphology 		4 0 4 1.0E-01 0 0
CUI: C1844813
Disease: Widely spaced teeth
Widely spaced teeth 		71 10 10 9.9E-02 3 0.18
CUI: C1844007
Disease: Corticospinal tract hypoplasia
Corticospinal tract hypoplasia 		5 0 4 9.8E-02 0 0
CUI: C3805574
Disease: Increased fracture rate
Increased fracture rate 		123 0 14 9.4E-02 0 0
CUI: C3279947
Disease: NAIL DISORDER, NONSYNDROMIC CONGENITAL, 9
NAIL DISORDER, NONSYNDROMIC CONGENITAL, 9 		77 0 10 9.3E-02 0 0
CUI: C0020608
Disease: Hypodontia
Hypodontia 		218 48 22 9.3E-02 1 1.8E-02
CUI: C0016038
Disease: Fibroelastosis
Fibroelastosis 		7 0 4 9.3E-02 0 0