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: C0010334
Disease: Crisscross Heart
Crisscross Heart
1 0 1 8.3E-02 0 0
CUI: C0232259
Disease: Mid-systolic murmur
Mid-systolic murmur
1 0 1 8.3E-02 0 0
CUI: C0265201
Disease: De Sanctis-Cacchione syndrome
De Sanctis-Cacchione syndrome
1 0 1 8.3E-02 0 0
CUI: C0349477
Disease: Transient neonatal hypothyroidism
Transient neonatal hypothyroidism
1 0 1 8.3E-02 0 0
Osteoarthritis of glenohumeral joint
1 0 1 8.3E-02 0 0
CUI: C0553668
Disease: Labored breathing
Labored breathing
1 0 1 8.3E-02 0 0
CUI: C0796093
Disease: Odontoonychodermal dysplasia
Odontoonychodermal dysplasia
1 0 1 8.3E-02 0 0
Central centrifugal cicatricial alopecia
1 0 1 8.3E-02 0 0
CUI: C1275074
Disease: Odonto-onycho-dermal dysplasia
Odonto-onycho-dermal dysplasia
1 0 1 8.3E-02 0 0
CUI: C1704335
Disease: Apocrine cystadenoma
Apocrine cystadenoma
1 0 1 8.3E-02 0 0
CUI: C1834056
Disease: Thin anteverted nares
Thin anteverted nares
1 0 1 8.3E-02 0 0
CUI: C1834057
Disease: Vertebral hyperostosis
Vertebral hyperostosis
1 0 1 8.3E-02 0 0
TOOTH AGENESIS, SELECTIVE, 4 (disorder)
1 0 1 8.3E-02 0 0
CUI: C1835493
Disease: Succedaneous Teeth, Agenesis Of
Succedaneous Teeth, Agenesis Of
1 0 1 8.3E-02 0 0
CUI: C1851095
Disease: Lumbosacral hirsutism
Lumbosacral hirsutism
1 0 1 8.3E-02 0 0
Subcortical white matter calcifications
1 0 1 8.3E-02 0 0
CUI: C1851431
Disease: Cerebellar calcifications
Cerebellar calcifications
1 0 1 8.3E-02 0 0
SCHOPF-SCHULZ-PASSARGE SYNDROME (disorder)
1 0 1 8.3E-02 0 0
CUI: C1857508
Disease: Patchy sclerosis of finger phalanx
Patchy sclerosis of finger phalanx
1 0 1 8.3E-02 0 0
CUI: C1857652
Disease: Thymic hormone decreased
Thymic hormone decreased
1 0 1 8.3E-02 0 0
Second metatarsal posteriorly placed
1 0 1 8.3E-02 0 0
CUI: C1860238
Disease: WOOLLY HAIR, AUTOSOMAL DOMINANT
WOOLLY HAIR, AUTOSOMAL DOMINANT
1 0 1 8.3E-02 0 0
CUI: C1861366
Disease: SYNDACTYLY, TYPE III
SYNDACTYLY, TYPE III
1 0 1 8.3E-02 0 0
Alopecia congenita keratosis palmoplantaris
1 0 1 8.3E-02 0 0
Oculodentodigital Dysplasia, Autosomal Recessive
1 0 1 8.3E-02 0 0