Congenital isolated acth 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
15476446 15613420
Orphanet —
CONGENITAL ISOLATED ADRENOCORTICOTROPIC HORMONE DEFICIENCY
MONDO:0008720C4055196
TBX19 Causal — ClinVar, GenCC, Disgenet —
All1 Causal1 Unknown1
Related Diseases Diseases that share the most curated genes with Congenital isolated acth deficiency.
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