OBO ID: DOID:0060347 |
Term Name: | acrorenal syndrome | Search Ontology: | |
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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 | ||
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Ontology: | Human Disease ( DOID:0060347 ) |
OTHER acrorenal syndrome PAGES
GENES INVOLVED
No data available
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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