Alopecia antibody deficiency (disorder) | | 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. | | syndroom van alopecia en antilichaamdeficiƫntie | | syndroom van alopecie en antilichaamdeficiƫntie syndroom van Ipp-Gelfand
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| Id | 783205005 | Status | Primitive |
DHD Diagnosis thesaurus reference set |
ICD-10 complex map reference set | Target | D80.8 | Rule | TRUE | Advice | ALWAYS D80.8 | 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 |
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