Congenital isolated adrenocorticotropic hormone deficiency

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Congenital isolated ACTH deficiency
199296
TBX19 Unknown
11290323 15476446 15613420
Orphanet, Open Targets —
All1 Causal1 Unknown1
Related Diseases Diseases that share the most curated genes with Congenital isolated adrenocorticotropic hormone deficiency.
4 View disease cluster →
Adrenocorticotropic hormone deficiency 1 shared geneTBX19 Related via 1 shared gene including TBX19. Duodenitis 1 shared geneTBX19 Related via 1 shared gene including TBX19. Pituitary stalk interruption syndrome 1 shared geneTBX19 Related via 1 shared gene including TBX19. Major depressive disorder 1 shared geneTBX19 Related via 1 shared gene including TBX19.