Baller-Gerold syndrome
synostosis characterized by coronal craniosynostosis, short stature, and aplasia or hypoplasia of the radial bone
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Baller-Gerold syndrome
Summary
Baller-Gerold syndrome is a developmental defect during embryogenesis[1]. It draws 42 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #123 of 308).[2]
Key Facts
- Baller-Gerold syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- Baller-Gerold syndrome's instance of is recorded as rare disease[4].
- Baller-Gerold syndrome's instance of is recorded as class of disease[5].
- Baller-Gerold syndrome is a type of synostosis[6].
- Baller-Gerold syndrome is a type of syndromic anorectal malformation[7].
- Baller-Gerold syndrome is a type of syndromic craniosynostosis[8].
- Baller-Gerold syndrome's genetic association is recorded as RECQL4[9].
- Baller-Gerold syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050654[10].
- Baller-Gerold syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0050654[11].
- Baller-Gerold syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1223[12].
- Baller-Gerold syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1225[13].
- Baller-Gerold syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
Why It Matters
Baller-Gerold syndrome draws 42 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #123 of 308).[2] It has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[15] It is known by 7 alternative names across languages and contexts.[16]