EF34EE1CA7FBBD024CBAEE6DB103997319996E1C14979DA77B490E73CE983D53B8EBBB38E0CE423DC12DF9148ACB1191

Defects in CDH3 are the cause of hypotrichosis with juvenile macular dystrophy (HJMD) [MIM:601553]. HJMD is a rare autosomal recessive disorder characterized by early hair loss heralding severe degenerative changes of the retinal macula and culminating in blindness during the second to third decade of life.

Source:http://purl.uniprot.org/SHA-384/EF34EE1CA7FBBD024CBAEE6DB103997319996E1C14979DA77B490E73CE983D53B8EBBB38E0CE423DC12DF9148ACB1191

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rdf:type	uniprot:Disease_Annotation
rdfs:comment	Defects in CDH3 are the cause of hypotrichosis with juvenile macular dystrophy (HJMD) [MIM:601553]. HJMD is a rare autosomal recessive disorder characterized by early hair loss heralding severe degenerative changes of the retinal macula and culminating in blindness during the second to third decade of life.