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bn:01245442n
Noun Concept
Categories: Congenital disorders, Autosomal recessive disorders, Genetic disorders with OMIM but no gene, Rare diseases, long volume value
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
Definitions
Relations
Sources
EN
Fibrochondrogenesis is a rare autosomal recessive form of osteochondrodysplasia, causing abnormal fibrous development of cartilage and related tissues. Wikipedia
Human disease Wikidata
IS A
rare disease
osteochondrodysplasia
GENETIC ASSOCIATION
COL11A2
Collagen, type XI, alpha 1
HEALTH SPECIALTY
medical genetics
Wikipedia
EN
fibrochondrogenesis
Wikidata
EN
fibrochondrogenesis
Wikidata Alias
EN
FBCG1, FIBROCHONDROGENESIS 1, FIBROCHONDROGENESIS 1; FBCG1, Fibrochondrogenesis type 1

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