Adrenocorticotropic hormone resistance syndrome	Autosomal recessive hereditary disorder	Congenital achalasia of esophagus	Digestive system hereditary disorder
\|	\|	\|	\|

Glucocorticoid deficiency with achalasia (disorder)
	Glucocorticoid deficiency with achalasia
	Achalasia-addisonian syndrome Triple A syndrome Alacrimia-achalasia-addisonianism Allgrove syndrome
	achalasie-addisonianisme-alacrimasyndroom
	triple-A-syndroom syndroom van Allgrove

Id	45414006
Status	Primitive

Finding site	Cardioesophageal junction structure
Occurrence	Congenital

Finding site	Adrenal cortex structure
Occurrence	Congenital

Has interpretation	Abnormal
Interprets	Motility

Finding site	Thyroid structure
Occurrence	Congenital

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	K22.0
Rule	TRUE
Advice	ALWAYS K22.0
Correlation	SNOMED CT source code to target map code correlation not specified

Target	E27.4
Rule	TRUE
Advice	ALWAYS E27.4
Correlation	SNOMED CT source code to target map code correlation not specified