Elig.phs000485.v1.p1.1
Item
Members of likely Mendelian families with apparent autosomal recessive or X-linked inheritance of congenital diaphragmatic hernia (CDH). Family history and genetic data were collected for every individual in the study. Additionally, a study geneticist performed a clinical assessment of the patients. Medical records were obtained and reviewed for every affected individual.
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C0235833 (UMLS CUI [1,1])
C0314657 (UMLS CUI [1,2])