acromesomele dysplasie	autosomaal dominante hereditaire aandoening	Genetic syndromic childhood obesity	hereditaire aandoening van bewegingsapparaat	hereditaire aandoening van endocrien systeem	hereditaire ontwikkelingsstoornis	metabole botziekte	pseudohypoparathyroïdie	verworven hypoparathyreoïdie
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pseudohypoparathyreoïdie type IA (aandoening)
	pseudohypoparathyreoïdie type IA
	PTH-resistentie type IA pseudohypoparathyroïdie type 1a syndroom van Albright type 1a
	Pseudohypoparathyroidism type I A
	Pseudohypoparathyroidism type Ia AHO - Albright hereditary osteodystrophy Albright hereditary osteodystrophy Albright hereditary osteodystrophy, classical type Pseudohypoparathyroidism type 1A

Id	58833000
Status	Primitive

Associated morphology	dysplasie
Finding site	botstructuur
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

Has interpretation	verlaagd
Interprets	hormoonsecretie

Occurrence

Finding site

structuur van bijschildklier

Has interpretation	boven referentiebereik
Interprets	meetbare observatie betreffende lichaamsgewicht

Global Patient Set

DHD Diagnosis thesaurus reference set

RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set

Target	E20.1
Term	Pseudohypoparathyroïdie

SNOMED CT to Orphanet simple map

79443

SNOMED CT to ICD-10 extended map

Target	E20.1
Rule	TRUE
Advice	ALWAYS E20.1 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified