OBO ID: DOID:0060347
Term Name: acrorenal syndrome Search Ontology:
Definition: A syndrome characterized by limb defects, usually bilateral, like cleft hands or feet and longitudinal defects involving radius or ulna, tibia or fibula and renal anomalies which include agenesis, hypoplasia and rarely polycystic kidneys. Additional malformations may involve the oro-mandibular region, the trachea and lungs, skin derivatives including sweat glands, mammary glands, the uterus, vas deferens, the nasal placodes and the eyes. https://www.ncbi.nlm.nih.gov/pubmed/26019842
Ontology: Human Disease   (DOID:0060347)
OTHER acrorenal syndrome PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available