autosomaal dominante hereditaire aandoening	ectodermale dysplasie	hereditaire aandoening van gebitselement	hereditaire aandoening van integumentum	hereditaire ontwikkelingsstoornis	neonataal gebitselement
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odontotricho-unguaal-digitopalmair syndroom (aandoening)
	odontotricho-unguaal-digitopalmair syndroom
	OTUDP-syndroom
	Odonto-tricho-ungual-digito-palmar syndrome
	Odontotrichoungual-digital-palmar syndrome Odonto-tricho-ungual-digito-palmar syndrome Mendoza-Valiente type
	This syndrome has characteristics of neonatal teeth, trichodystrophy and malformations of the hands and feet. To date, it has been reported in 21 patients and is transmitted as an autosomal dominant trait.

Id	722063009
Status	Primitive

Associated morphology	morfologische afwijking
Finding site	structuur van huid
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

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

Associated morphology	versnelde maturatie
Finding site	structuur van gebitselement
Occurrence	neonataal

Has interpretation	afwijkend
Interprets	Eruption of tooth

DHD Diagnosis thesaurus reference set

RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set

Target	Q87.8
Term	Overige gespecificeerde congenitale gestoorde-ontwikkelingssyndromen, niet elders geclassificeerd

SNOMED CT to Orphanet simple map

69082

SNOMED CT to ICD-10 extended map

Target	Q87.8
Rule	TRUE
Advice	ALWAYS Q87.8 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified