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: C0013338
Disease: Pituitary dwarfism
Pituitary dwarfism
41 12 6 0.15 1 2.9E-02
CUI: C0266677
Disease: Synotus
Synotus
2 0 1 0.14 0 0
Facial Dysmorphism with Multiple Malformations
2 0 1 0.14 0 0
PITUITARY HORMONE DEFICIENCY, COMBINED, 4
2 0 1 0.14 0 0
CUI: C2910315
Disease: Split foot, bilateral
Split foot, bilateral
2 0 1 0.14 0 0
CUI: C3151380
Disease: SCHIZOPHRENIA 15
SCHIZOPHRENIA 15
2 0 1 0.14 0 0
Anterior pituitary hormone deficiency
2 0 1 0.14 0 0
CUI: C4014479
Disease: CULLER-JONES SYNDROME
CULLER-JONES SYNDROME
2 0 1 0.14 0 0
CUI: C4020815
Disease: Agenesis of incisor
Agenesis of incisor
2 0 1 0.14 0 0
Absence of secondary sex characteristics
44 0 6 0.14 0 0
Follicle stimulating hormone deficiency
11 0 2 0.13 0 0
CUI: C3665349
Disease: Secondary hypothyroidism
Secondary hypothyroidism
47 0 6 0.13 0 0
CUI: C0018987
Disease: Hemimelia
Hemimelia
3 0 1 0.12 0 0
Isolated Growth Hormone Deficiency, Type II
3 0 1 0.12 0 0
CUI: C0333317
Disease: Fibrous body
Fibrous body
3 0 1 0.12 0 0
CUI: C1395317
Disease: Dextrocardia with situs inversus
Dextrocardia with situs inversus
3 0 1 0.12 0 0
CUI: C1868549
Disease: Marked delay in bone age
Marked delay in bone age
3 0 1 0.12 0 0
CUI: C1876185
Disease: Dysgnathia complex
Dysgnathia complex
3 0 1 0.12 0 0
CUI: C2748860
Disease: Hypoplastic pituitary gland
Hypoplastic pituitary gland
3 0 1 0.12 0 0
CUI: C4020770
Disease: Hypoplasia of the premaxilla
Hypoplasia of the premaxilla
3 0 1 0.12 0 0
CUI: C4046049
Disease: Anti-PIT-1 Antibody Syndrome
Anti-PIT-1 Antibody Syndrome
3 0 1 0.12 0 0
CUI: C0265242
Disease: Otocephaly
Otocephaly
4 0 1 0.11 0 0
CUI: C0266215
Disease: Anorectal atresia
Anorectal atresia
4 0 1 0.11 0 0
CUI: C0398370
Disease: Lipedema
Lipedema
4 0 1 0.11 0 0
CUI: C1833798
Disease: Optic Nerve Aplasia, Bilateral
Optic Nerve Aplasia, Bilateral
4 0 1 0.11 0 0