hereditary disease phocomelia-ectrodactyly-deafness-sinus arrhythmia syndrome https://github.com/monarch-initiative/mondo/issues/6877 https://www.malacards.org/card/phocomelia_ectrodactyly_ear_malformation_deafness_and_sinus_arrhythmia_2 Stoll-LC)vy-Francfort syndrome Stoll-levy-Francfort syndrome phocomelia ectrodactyly deafness sinus arrhythmia MONDO:0008237 GARD:0004323 MEDGEN:356961 OMIM:171480 MESH:C537498 Phocomelia-ectrodactyly-deafness-sinus arrhythmia syndrome is characterized by phocomelia (involving arms more severely), ectrodactyly, ear anomalies (bilateral anomalies of the pinnae), conductive deafness, dysmorphism (long and prominent philtrum, mild maxillary hypoplasia) and sinus arrhythmia. It has been described in four patients (a father and his son and a mother and her daughter) from two unrelated families. UMLS:C1868390 Stoll-Lévy-Francfort syndrome Orphanet:2878 dysostosis congenital limb malformation