congenital bilateral aplasia of the vas deferens
human disease
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congenital bilateral aplasia of the vas deferens
Summary
congenital bilateral aplasia of the vas deferens is a developmental defect during embryogenesis[1].
Key Facts
- congenital bilateral aplasia of the vas deferens's instance of is recorded as developmental defect during embryogenesis[2].
- congenital bilateral aplasia of the vas deferens's instance of is recorded as rare disease[3].
- congenital bilateral aplasia of the vas deferens's instance of is recorded as class of disease[4].
- congenital bilateral aplasia of the vas deferens is a type of congenital aplasia of the vas deferens[5].
- congenital bilateral aplasia of the vas deferens is a type of X-linked disease[6].
- congenital bilateral aplasia of the vas deferens is a type of azoospermia[7].
- congenital bilateral aplasia of the vas deferens's NCI Thesaurus ID is recorded as C129303[8].
- congenital bilateral aplasia of the vas deferens's genetic association is recorded as CFTR[9].
- congenital bilateral aplasia of the vas deferens's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_48[10].
- congenital bilateral aplasia of the vas deferens's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111862[11].
- congenital bilateral aplasia of the vas deferens's exact match is recorded as http://identifiers.org/doid/DOID:0111862[12].