chondrodysplasia Blomstrand type
Human disease
Press Enter · cited answer in seconds
0 sources
chondrodysplasia Blomstrand type
Summary
chondrodysplasia Blomstrand type is a developmental defect during embryogenesis[1].
Key Facts
- chondrodysplasia Blomstrand type's instance of is recorded as developmental defect during embryogenesis[2].
- chondrodysplasia Blomstrand type's instance of is recorded as rare disease[3].
- chondrodysplasia Blomstrand type's instance of is recorded as class of disease[4].
- chondrodysplasia Blomstrand type is a type of osteochondrodysplasia[5].
- chondrodysplasia Blomstrand type is a type of neonatal osteosclerotic dysplasia[6].
- chondrodysplasia Blomstrand type's NCI Thesaurus ID is recorded as C131420[7].
- chondrodysplasia Blomstrand type's genetic association is recorded as PTH1R[8].
- chondrodysplasia Blomstrand type's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060387[9].
- chondrodysplasia Blomstrand type's exact match is recorded as http://identifiers.org/doid/DOID:0060387[10].
- chondrodysplasia Blomstrand type's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_50945[11].
- chondrodysplasia Blomstrand type's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].