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: C0013338
Disease: Pituitary dwarfism
Pituitary dwarfism 		41 12 13 0.12 1 5.6E-02
CUI: C0271561
Disease: Somatotropin deficiency
Somatotropin deficiency 		154 0 24 0.11 0 0
CUI: C0271568
Disease: Laron Syndrome
Laron Syndrome 		20 0 10 0.11 0 0
CUI: C0744483
Disease: growth hormone treatment
growth hormone treatment 		20 0 10 0.11 0 0
CUI: C3714796
Disease: Isolated somatotropin deficiency
Isolated somatotropin deficiency 		168 0 24 0.11 0 0
CUI: C0015544
Disease: Failure to Thrive
Failure to Thrive 		842 10 83 9.8E-02 6 0.55
CUI: C1837475
Disease: Insulin-Like Growth Factor I Deficiency
Insulin-Like Growth Factor I Deficiency 		28 0 10 9.8E-02 0 0
CUI: C0043116
Disease: HMN (Hereditary Motor Neuropathy) Proximal Type I
HMN (Hereditary Motor Neuropathy) Proximal Type I 		34 0 10 9.3E-02 0 0
CUI: C0001080
Disease: Achondroplasia
Achondroplasia 		46 0 11 9.2E-02 0 0
CUI: C3665349
Disease: Secondary hypothyroidism
Secondary hypothyroidism 		47 0 11 9.2E-02 0 0
CUI: C0342388
Disease: Adrenocorticotropic hormone (ACTH) deficiency (disorder)
Adrenocorticotropic hormone (ACTH) deficiency (disorder) 		24 0 9 9.1E-02 0 0
CUI: C0020635
Disease: Hypopituitarism
Hypopituitarism 		69 0 12 8.5E-02 0 0
CUI: C0268141
Disease: Xeroderma pigmentosum, group G
Xeroderma pigmentosum, group G 		20 0 8 8.3E-02 0 0
CUI: C0271801
Disease: Central hypothyroidism
Central hypothyroidism 		35 0 9 8.2E-02 0 0
CUI: C4304411
Disease: Xeroderma pigmentosum and Cockayne syndrome complex
Xeroderma pigmentosum and Cockayne syndrome complex 		10 0 7 8.0E-02 0 0
CUI: C0018273
Disease: Growth Disorders
Growth Disorders 		39 0 9 7.9E-02 0 0
CUI: C0268136
Disease: Xeroderma pigmentosum, group B
Xeroderma pigmentosum, group B 		13 0 7 7.8E-02 0 0
CUI: C0035613
Disease: Rift Valley Fever
Rift Valley Fever 		45 0 9 7.5E-02 0 0
CUI: C0346302
Disease: Growth Hormone-Secreting Pituitary Adenoma
Growth Hormone-Secreting Pituitary Adenoma 		60 0 10 7.5E-02 0 0
CUI: C1955934
Disease: Trichothiodystrophy Syndromes
Trichothiodystrophy Syndromes 		33 0 8 7.3E-02 0 0
CUI: C0268135
Disease: Xeroderma pigmentosum, group A
Xeroderma pigmentosum, group A 		48 0 9 7.3E-02 0 0
CUI: C0043346
Disease: Xeroderma Pigmentosum
Xeroderma Pigmentosum 		137 0 15 7.3E-02 0 0
CUI: C0010276
Disease: Craniopharyngioma
Craniopharyngioma 		64 0 10 7.2E-02 0 0
CUI: C0205770
Disease: Choroid Plexus Papilloma
Choroid Plexus Papilloma 		64 0 10 7.2E-02 0 0
CUI: C0338503
Disease: Septo-Optic Dysplasia
Septo-Optic Dysplasia 		35 0 8 7.2E-02 0 0