<owl:Class xmlns="https://folio.openlegalstandard.org/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:v1="http://www.loc.gov/mads/rdf/v1#" xmlns:owl="http://www.w3.org/2002/07/owl#" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:xsd="http://www.w3.org/2001/XMLSchema#" xmlns:folio="https://folio.openlegalstandard.org/" xmlns:rdfs="http://www.w3.org/2000/01/rdf-schema#" xmlns:skos="http://www.w3.org/2004/02/skos/core#" rdf:about="https://folio.openlegalstandard.org/R7e0Y5id3RWAv0exuZTef8d">
  <rdfs:subClassOf rdf:resource="https://folio.openlegalstandard.org/R8LxIR1bsgFd3td2G24G3mq"/>
  <rdfs:label>Caudal Regression Syndrome</rdfs:label>
  <skos:altLabel>CRS</skos:altLabel>
  <skos:altLabel>Caudal Dysgenesis</skos:altLabel>
  <skos:altLabel>Sacral Agenesis</skos:altLabel>
  <skos:definition>Caudal Regression Syndrome (CRS) is a rare congenital disorder that results from abnormal development of the lower spine and structures. It affects the development of the caudal (tail) region of the embryo, leading to a spectrum of anomalies involving the lower spinal cord, pelvis, and lower limbs.</skos:definition>
</owl:Class>
