alopecia totalis	deficiëntie van specifiek antilichaam
\|	\|

syndroom van alopecia en antilichaamdeficiëntie (aandoening)
	syndroom van alopecia en antilichaamdeficiëntie
	syndroom van alopecie en antilichaamdeficiëntie syndroom van Ipp-Gelfand
	Alopecia antibody deficiency
	Ipp Gelfand syndrome
	A rare primary immunodeficiency disorder characterized by the association of alopecia areata totalis and antibody deficiency (congenital agammaglobulinemia or incomplete antibody deficiency syndrome) manifesting with recurrent infections. There have been no further descriptions in the literature since 1976.

Id	783205005
Status	Primitive

Associated morphology	afwezigheid
Finding site	structuur van pilus

Finding site	structuur van immuunsysteem
Pathological process	afwijkend immuunproces

DHD Diagnosis thesaurus reference set

RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set

Target	D80.8
Term	Overige gespecificeerde immunodeficiënties met overwegend antilichaamstoornissen

Target	L63.0
Term	Alopecia (capitis) totalis

SNOMED CT to Orphanet simple map

1006

SNOMED CT to ICD-10 extended map

Target	D80.8
Rule	TRUE
Advice	ALWAYS D80.8 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified

Target	L63.0
Rule	TRUE
Advice	ALWAYS L63.0
Correlation	SNOMED CT source code to target map code correlation not specified