has material basis in germline mutation in disease has feature SLC39A4 Abnormal eyebrow morphology inborn metal metabolism disorder intestinal disorder skin disorder acrodermatitis enteropathica https://github.com/monarch-initiative/mondo/issues/5682 https://rarediseases.info.nih.gov/diseases/5723/acrodermatitis-enteropathica https://rarediseases.info.nih.gov/diseases/6343/enteropathica https://www.malacards.org/card/acrodermatitis_enteropathica https://www.malacards.org/card/acrodermatitis_enteropathica_zinc_deficiency_type acrodermatitis enteropathica, zinc-deficiency type Acrodermatitis enteropathica (AE) is a rare inherited inborn error of metabolism resulting in a severe zinc deficiency and characterized by acral dermatitis, alopecia, diarrhea and growth failure. ae MEDGEN:66355 Orphanet:37 Danbolt-Cross syndrome icd11.foundation:1813939482 acrodermatitis enteropathica zinc deficiency type acrodermatitis enteropathica, zinc deficiency type MESH:C538178 SCTID:37702000 ICD9:686.8 GARD:0005723 MONDO:0008713 Brandt syndrome inherited zinc deficiency OMIM:201100 enteropathica acrodermatitis enteropathica DOID:0050605 NORD:721 NCIT:C128802 UMLS:C0221036 MONDO:0023070 NANDO:2200584 AEZ disorder of zinc metabolism