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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
Fraser syndrome +     
Fraser syndrome 1  
Rare autosomal recessive congenital malformation syndrome characterized by cryptophthalmos, SYNDACTYLY and UROGENITAL ABNORMALITIES. Other anomalies of bone, ear, lung, and nose are common. Mutations on FRAS1 and FREM2 are associated with the syndrome.
Fraser syndrome 2  
Fraser syndrome 3  

Synonyms
Exact Synonyms: CRYPTOPHTHALMOS SYNDROME ;   FRASRS1
Primary IDs: OMIM:219000
Alternate IDs: DOID:9000526
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/12766769 "DO"

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.