DO_rare_slim has phenotype ectodermal dysplasia and immune deficiency MIM:PS300291 DOID:0081077 GARD:9936 disease_ontology An ectodermal dysplasia syndrome that is characterized by signs of ectodermal dysplasia (sparse hair, abnormal or missing teeth, decrease or absent sudation), typical facial features (protruding forehead, wrinkles under the eyes, characteristic periorbital hyperpigmentation), and immunodeficiency. Anhidrotic ectodermal dysplasia with immune deficiency Ectodermal dysplasia, hypohidrotic, with immune deficiency ectodermal dysplasia primary immunodeficiency disease Abnormality of immune system physiology