syndromic disease mullerian derivatives-lymphangiectasia-polydactyly syndrome https://github.com/monarch-initiative/mondo/issues/6878 https://www.malacards.org/card/mullerian_derivatives_lymphangiectasia_polydactyly_syndrome https://www.malacards.org/card/mullerian_derivatives_persistence_of_with_lymphangiectasia_and_postaxial_polydactyly MESH:C536478 renal and craniofacial anomalies with persistence of mullerian derivatives, lymphangiectasis, hepatic failure, postaxial polydactyly Orphanet:1655 OMIM:235255 GARD:0005430 UMLS:C1856159 MEDGEN:343489 persistence of mullerian derivatives with lymphangiectasia and postaxial polydactyly Mullerian derivatives-lymphangiectasia-polydactyly syndrome is characterized by prenatal linear growth deficiency, hypertrophied alveolar ridges, redundant nuchal skin, postaxial polydactyly and cryptorchidism. Mullerian duct remnants, lymphangiectasis, and renal anomalies are also present. Three cases have been described. A small penis was observed in two of these cases. The syndrome is likely to be an autosomal recessive or X-linked trait. All the reported patients died neonatally of hepatic failure. MONDO:0009333 primary lymphedema