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: C0877018
Disease: Pituitary enlargement
Pituitary enlargement 		1 0 1 0.17 0 0
CUI: C0878683
Disease: Pituitary Dwarfism Type 3
Pituitary Dwarfism Type 3 		1 0 1 0.17 0 0
CUI: C1835819
Disease: PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES (disorder)
PITUITARY ANOMALIES WITH HOLOPROSENCEPHALY-LIKE FEATURES (disorder) 		1 0 1 0.17 0 0
CUI: C1864690
Disease: Microphthalmia, Syndromic 5
Microphthalmia, Syndromic 5 		1 0 1 0.17 0 0
CUI: C2750027
Disease: Growth Hormone Deficiency With Pituitary Anomalies
Growth Hormone Deficiency With Pituitary Anomalies 		1 0 1 0.17 0 0
CUI: C2930844
Disease: Hypopituitarism and septooptic 'dysplasia'
Hypopituitarism and septooptic 'dysplasia' 		1 0 1 0.17 0 0
CUI: C3151440
Disease: PITUITARY HORMONE DEFICIENCY, COMBINED, 6
PITUITARY HORMONE DEFICIENCY, COMBINED, 6 		1 0 1 0.17 0 0
CUI: C3804969
Disease: Dysgnathia
Dysgnathia 		1 0 1 0.17 0 0
CUI: C4305151
Disease: Syndromic microphthalmia type 5
Syndromic microphthalmia type 5 		1 0 1 0.17 0 0
CUI: C0266677
Disease: Synotus
Synotus 		2 0 1 0.14 0 0
CUI: C1856892
Disease: Facial Dysmorphism with Multiple Malformations
Facial Dysmorphism with Multiple Malformations 		2 0 1 0.14 0 0
CUI: C2678408
Disease: PITUITARY HORMONE DEFICIENCY, COMBINED, 4
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
CUI: C3875161
Disease: Anterior pituitary hormone deficiency
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
CUI: C0018987
Disease: Hemimelia
Hemimelia 		3 0 1 0.12 0 0
CUI: C0271567
Disease: Isolated Growth Hormone Deficiency, Type II
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