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: C1858656
Disease: Short Stature, Idiopathic, Autosomal
Short Stature, Idiopathic, Autosomal 		3 0 2 0.20 0 0
CUI: C4023211
Disease: Adrenocorticotropin deficient adrenal insufficiency
Adrenocorticotropin deficient adrenal insufficiency 		6 0 2 0.15 0 0
CUI: C0268248
Disease: Niemann-Pick Disease, Type E
Niemann-Pick Disease, Type E 		1 0 1 0.11 0 0
CUI: C0276429
Disease: Enteroviral encephalomyelitis
Enteroviral encephalomyelitis 		1 0 1 0.11 0 0
CUI: C0338401
Disease: Enteroviral encephalitis
Enteroviral encephalitis 		1 0 1 0.11 0 0
CUI: C0476337
Disease: Blood gases abnormal
Blood gases abnormal 		1 0 1 0.11 0 0
CUI: C0855232
Disease: Markedly reduced food intake
Markedly reduced food intake 		1 0 1 0.11 0 0
CUI: C1400201
Disease: Pituitary anomalies
Pituitary anomalies 		1 0 1 0.11 0 0
CUI: C1843428
Disease: Diffuse reticular or finely nodular infiltrations
Diffuse reticular or finely nodular infiltrations 		1 0 1 0.11 0 0
CUI: C1855548
Disease: Laron syndrome type 2
Laron syndrome type 2 		1 6 1 0.11 3 0.50
CUI: C2675463
Disease: Chromosome 15q26-Qter Deletion Syndrome
Chromosome 15q26-Qter Deletion Syndrome 		1 0 1 0.11 0 0
CUI: C2675646
Disease: NIEMANN-PICK DISEASE, INTERMEDIATE, PROTRACTED NEUROVISCERAL (disorder)
NIEMANN-PICK DISEASE, INTERMEDIATE, PROTRACTED NEUROVISCERAL (disorder) 		1 0 1 0.11 0 0
CUI: C2721740
Disease: Ventilation perfusion mismatch
Ventilation perfusion mismatch 		1 0 1 0.11 0 0
CUI: C3165091
Disease: Double outlet right ventricle with doubly committed ventricular septal defect and pulmonary stenosis
Double outlet right ventricle with doubly committed ventricular septal defect and pulmonary stenosis 		1 0 1 0.11 0 0
CUI: C3888131
Disease: INCREASED RESPONSIVENESS TO GROWTH HORMONE
INCREASED RESPONSIVENESS TO GROWTH HORMONE 		1 0 1 0.11 0 0
CUI: C4016705
Disease: LARON SYNDROME WITH ELEVATED SERUM GH-BINDING PROTEIN
LARON SYNDROME WITH ELEVATED SERUM GH-BINDING PROTEIN 		1 0 1 0.11 0 0
CUI: C4016706
Disease: LARON SYNDROME WITH UNDETECTABLE SERUM GH-BINDING PROTEIN
LARON SYNDROME WITH UNDETECTABLE SERUM GH-BINDING PROTEIN 		1 0 1 0.11 0 0
CUI: C4020789
Disease: Abnormal sperm development
Abnormal sperm development 		1 0 1 0.11 0 0
CUI: C4021966
Disease: Abnormality of the periungual region
Abnormality of the periungual region 		1 0 1 0.11 0 0
CUI: C4022874
Disease: Abnormal size of pituitary gland
Abnormal size of pituitary gland 		1 0 1 0.11 0 0
CUI: C4321359
Disease: Reduced insulin like growth factor binding protein acid labile subunit level
Reduced insulin like growth factor binding protein acid labile subunit level 		1 0 1 0.11 0 0
CUI: C4331952
Disease: STAT5B Deficiency
STAT5B Deficiency 		1 0 1 0.11 0 0
CUI: C4476848
Disease: Low 1-minute APGAR score
Low 1-minute APGAR score 		1 0 1 0.11 0 0
CUI: C1864570
Disease: Insulin insensitivity
Insulin insensitivity 		2 0 1 1.0E-01 0 0
CUI: C2677535
Disease: Alopecia, Neurologic Defects, and Endocrinopathy Syndrome
Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 		2 0 1 1.0E-01 0 0