has material basis in germline mutation in FERMT1 Kindler syndrome https://www.malacards.org/card/kindler_syndrome DOID:0060472 MESH:C536321 bullous acrokeratotic poikiloderma of Kindler and Weary Kindler syndrome MONDO:0008260 GARD:0004391 poikiloderma of Kindler poikiloderma, congenital, with bullae, Weary type OMIM:173650 KINDLER syndrome UMLS:C0406557 KNDLRS KS NANDO:1200239 SCTID:238836000 icd11.foundation:726317303 Kindler syndrome (KS) is the fourth major type of epidermolysis bullosa (EB), besides simplex, junctional and dystrophic forms, and is characterized by skin fragility and blistering at birth followed by development of photosensitivity and progressive poikilodermatous skin changes. Orphanet:2908 MEDGEN:96060 congenital bullous poikiloderma poikiloderma, hereditary acrokeratotic inherited epidermolysis bullosa