metaphyseal dysplasia-maxillary hypoplasia-brachydacty syndrome
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metaphyseal dysplasia-maxillary hypoplasia-brachydacty syndrome
Summary
metaphyseal dysplasia-maxillary hypoplasia-brachydacty syndrome is a developmental defect during embryogenesis[1].
Key Facts
- metaphyseal dysplasia-maxillary hypoplasia-brachydacty syndrome's instance of is recorded as developmental defect during embryogenesis[2].
- metaphyseal dysplasia-maxillary hypoplasia-brachydacty syndrome's instance of is recorded as rare disease[3].
- metaphyseal dysplasia-maxillary hypoplasia-brachydacty syndrome's instance of is recorded as class of disease[4].
- metaphyseal dysplasia-maxillary hypoplasia-brachydacty syndrome is a type of multiple metaphyseal dysplasia[5].
- metaphyseal dysplasia-maxillary hypoplasia-brachydacty syndrome is a type of osteochondrodysplasia[6].
- metaphyseal dysplasia-maxillary hypoplasia-brachydacty syndrome is a type of autosomal dominant disease[7].
- metaphyseal dysplasia-maxillary hypoplasia-brachydacty syndrome's genetic association is recorded as RUNX2[8].
- metaphyseal dysplasia-maxillary hypoplasia-brachydacty syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2504[9].
- metaphyseal dysplasia-maxillary hypoplasia-brachydacty syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111513[10].
- metaphyseal dysplasia-maxillary hypoplasia-brachydacty syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0111513[11].