acrofacial dysostosis, Weyers type
human disease
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acrofacial dysostosis, Weyers type
Summary
acrofacial dysostosis, Weyers type is a developmental defect during embryogenesis[1].
Key Facts
- acrofacial dysostosis, Weyers type's instance of is recorded as developmental defect during embryogenesis[2].
- acrofacial dysostosis, Weyers type's instance of is recorded as rare disease[3].
- acrofacial dysostosis, Weyers type's instance of is recorded as class of disease[4].
- acrofacial dysostosis, Weyers type is a type of multiple congenital anomalies/dysmorphic syndrome without intellectual disability[5].
- acrofacial dysostosis, Weyers type is a type of branchial arch or oral-acral syndrome[6].
- acrofacial dysostosis, Weyers type is a type of acrofacial dysostosis[7].
- acrofacial dysostosis, Weyers type is a type of autosomal dominant disease[8].
- acrofacial dysostosis, Weyers type's ICD-9-CM is recorded as 520.8[9].
- acrofacial dysostosis, Weyers type's genetic association is recorded as EVC[10].
- acrofacial dysostosis, Weyers type's genetic association is recorded as EVC2[11].
- acrofacial dysostosis, Weyers type's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_952[12].
- acrofacial dysostosis, Weyers type's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111571[13].
- acrofacial dysostosis, Weyers type's exact match is recorded as http://identifiers.org/doid/DOID:0111571[14].