has material basis in germline mutation in WAS X-linked disease skin disorder Wiskott-Aldrich syndrome https://github.com/monarch-initiative/mondo/issues/4521 https://rarediseases.info.nih.gov/diseases/7895/wiskott-aldrich-syndrome https://www.malacards.org/card/wiskott_aldrich_syndrome SCTID:36070007 NCIT:C3448 Wiskott-Aldrich syndrome, X-linked recessive immunodeficiency 2 GARD:0007895 Wiskott-Aldrich syndrome (WAS) is a primary immunodeficiency disease characterized by microthrombocytopenia, eczema, infections and an increased risk for autoimmune manifestations and malignancies. ICD10CM:D82.0 Wiskott Aldrich syndrome Aldrich syndrome UMLS:C0043194 Wiskott-Aldrich syndrome 1 MEDGEN:21921 DOID:9169 NANDO:1200330 MedDRA:10047992 MONDO:0010518 icd11.foundation:168952525 OMIM:301000 Imd 2 eczema thrombocytopenia immunodeficiency syndrome Wiskott-Aldrich syndrome MESH:D014923 NANDO:2200704 ICD9:279.12 eczema-thrombocytopenia-immunodeficiency syndrome WAS Orphanet:906 combined immunodeficiency hereditary neoplastic syndrome inherited blood coagulation disorder