has material basis in germline mutation in TERC dyskeratosis congenita, autosomal dominant 1 https://rarediseases.info.nih.gov/diseases/6299/dyskeratosis-congenita-autosomal-dominant https://www.malacards.org/card/dyskeratosis_congenita_autosomal_dominant_1 dyskeratosis congenita, Scoggins type OMIM:127550 SCTID:707273001 DKCA dyskeratosis congenita autosomal dominant DOID:0070014 autosomal dominant dyskeratosis congenita dyskeratosis congenita, autosomal dominant type 1 MEDGEN:1645250 autosomal dominant dyskeratosis congenita 1 GARD:0006299 dyskeratosis congenita Scoggins type A dyskeratosis congenita that has material basis in an autosomal dominant mutation of TERC on chromosome 3q26.2. NCIT:C176921 MESH:C565079 DKCA1 UMLS:C4551974 MONDO:0007485 dyskeratosis congenita, autosomal dominant 1 dyskeratosis congenita telomere syndrome