bn:01245442n
Noun Concept
Categories: Rare diseases, Congenital disorders, long volume value, Genetic disorders with OMIM but no gene, Autosomal recessive disorders
EN
fibrochondrogenesis  FBCG1  FIBROCHONDROGENESIS 1  FIBROCHONDROGENESIS 1; FBCG1  Fibrochondrogenesis type 1
EN
Fibrochondrogenesis is a rare autosomal recessive form of osteochondrodysplasia, causing abnormal fibrous development of cartilage and related tissues. Wikipedia
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EN
Fibrochondrogenesis is a rare autosomal recessive form of osteochondrodysplasia, causing abnormal fibrous development of cartilage and related tissues. Wikipedia
Human disease Wikidata