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FGFR3-related chondrodysplasia

MedGen UID:
833115
Concept ID:
CN229200
Finding
Monarch Initiative: MONDO:0019685
Orphanet: ORPHA93420

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • FGFR3-related chondrodysplasia
Follow this link to review classifications for FGFR3-related chondrodysplasia in Orphanet.

Recent clinical studies

Diagnosis

Hasegawa K, Tanaka H
Pediatr Int 2014 Dec;56(6):809-812. Epub 2014 Nov 28 doi: 10.1111/ped.12511. PMID: 25244068

Clinical prediction guides

Hasegawa K, Tanaka H
Pediatr Int 2014 Dec;56(6):809-812. Epub 2014 Nov 28 doi: 10.1111/ped.12511. PMID: 25244068

Supplemental Content

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    Clinical resources

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