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's subclass of is recorded as multiple congenital anomalies/dysmorphic syndrome without intellectual disability^[5].
• acrofacial dysostosis, Weyers type's subclass of is recorded as branchial arch or oral-acral syndrome^[6].
• acrofacial dysostosis, Weyers type's subclass of is recorded as acrofacial dysostosis^[7].
• acrofacial dysostosis, Weyers type's subclass of is recorded as autosomal dominant disease^[8].
• acrofacial dysostosis, Weyers type's MeSH descriptor ID is recorded as C536695^[9].
• acrofacial dysostosis, Weyers type's OMIM ID is recorded as 193530^[10].
• acrofacial dysostosis, Weyers type's KEGG ID is recorded as H02158^[11].
• acrofacial dysostosis, Weyers type's Disease Ontology ID is recorded as DOID:0111571^[12].
• acrofacial dysostosis, Weyers type's Orphanet ID is recorded as 952^[13].
• acrofacial dysostosis, Weyers type's ICD-9-CM is recorded as 520.8^[14].
• acrofacial dysostosis, Weyers type's genetic association is recorded as EVC^[15].
• acrofacial dysostosis, Weyers type's genetic association is recorded as EVC2^[16].
• acrofacial dysostosis, Weyers type's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_952^[17].
• acrofacial dysostosis, Weyers type's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111571^[18].
• acrofacial dysostosis, Weyers type's exact match is recorded as http://identifiers.org/doid/DOID:0111571^[19].
• acrofacial dysostosis, Weyers type's UMLS CUI is recorded as C0457013^[20].
• acrofacial dysostosis, Weyers type's ICD-10-CM is recorded as Q75.4^[21].
• acrofacial dysostosis, Weyers type's GARD rare disease ID is recorded as 497^[22].
• acrofacial dysostosis, Weyers type's Mondo ID is recorded as MONDO_0008673^[23].
• acrofacial dysostosis, Weyers type's Genetics Home Reference Conditions ID is recorded as weyers-acrofacial-dysostosis^[24].
• acrofacial dysostosis, Weyers type's ICD-11 ID is recorded as 547338814^[25].
• acrofacial dysostosis, Weyers type's UniProt disease ID is recorded as DI-00029^[26].