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Diseases / Disease of genetic or genomic mechanism/ Hereditary disease/ Skeletal dysplasia

FGFR3-related chondrodysplasia

rare

Identifiers: MONDO:0019685 Orphanet:93420
Part of: Skeletal dysplasia

Subtypes

All diseases Rare only

Disease Rare Not rare Subtypes

Thanatophoric dysplasia MONDO:0017042 FGFR3 5
Achondroplasia MONDO:0007037 FGFR3
Camptodactyly-tall stature-scoliosis-hearing loss syndrome MONDO:0012504 FGFR3
Hypochondroplasia MONDO:0007793 FGFR3
Severe achondroplasia-developmental delay-acanthosis nigricans syndrome MONDO:0014658 FGFR3

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