has characteristic has characteristic has material basis in germline mutation in SMARCAD1 absence of fingerprints-congenital milia syndrome https://github.com/monarch-initiative/mondo/issues/4069 https://rarediseases.info.nih.gov/diseases/2336/absence-of-fingerprints-congenital-milia https://www.malacards.org/card/absence_of_fingerprints_congenital_milia_syndrome https://www.malacards.org/card/basan_syndrome OMIM:129200 Basan syndrome SCTID:239011004 absence of dermatoglyphics congenital milia GARD:0002336 icd11.foundation:1298640608 absence of dermatoglyphics-congenital milia syndrome Baird syndrome MEDGEN:140808 DOID:0080725 absence of fingerprints congenital milia MESH:C537659 MONDO:0007507 UMLS:C0406707 Absence of fingerprints-congenital milia syndrome is characterized by neonatal blisters and milia (small white papules, especially on the face) and congenital absence of dermatoglyphics on the hands and feet. It has been reported in two kindreds (one of which contained 13 affected individuals spanning three generations) and in an unrelated individual. Some affected patients also showed bilateral partial flexion contractures of the fingers and toes, and webbing of the toes. The syndrome is inherited as an autosomal dominant trait. adermatoglyphia with congenital facial milia and acral blisters, digital contractures, and nail abnormalities Orphanet:1658 epidermal disease congenital hereditary skin disorder