eDiPNet

Subtype of: Albright hereditary osteodystrophy · Intellectual disability

Show by gene (one row per gene, with all of its disease terms together)

Pathways column key: KEGG Reactome

Disease Term	Disease ID	Gene Symbol	Classification	References	Source	Pathways
Albright hereditary osteodystrophy type 3	MONDO_0010886	HDAC4	Unknown	25402011 19365831 20691407 15521982	Open Targets	Apelin signaling pathway Neutrophil extracellular trap formation Alcoholism +8 more
Albright hereditary osteodystrophy type 3, Albright hereditary osteodystrophy-like syndrome, Brachydactyly-intellectual disability, Del(2)(q37)	MONDO_0010886	HDAC4	Unknown	25402011 19365831 20691407 15521982 30848064	Open Targets	Apelin signaling pathway Neutrophil extracellular trap formation Alcoholism +8 more
Albright hereditary osteodystrophy-like syndrome	MONDO_0010886	HDAC4	Unknown	25402011 19365831 20691407 15521982	Open Targets	Apelin signaling pathway Neutrophil extracellular trap formation Alcoholism +8 more

Albright hereditary osteodystrophy type 3