craniofrontonasal dysplasia
human disease
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Summary
craniofrontonasal dysplasia is a developmental defect during embryogenesis[1]. It draws 148 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #83 of 308).[2]
Key Facts
- craniofrontonasal dysplasia's instance of is recorded as developmental defect during embryogenesis[3].
- craniofrontonasal dysplasia's instance of is recorded as rare disease[4].
- craniofrontonasal dysplasia's instance of is recorded as class of disease[5].
- craniofrontonasal dysplasia is a type of X-linked intellectual disability[6].
- craniofrontonasal dysplasia is a type of X-linked dominant disease[7].
- craniofrontonasal dysplasia is a type of midface dysplasia[8].
- craniofrontonasal dysplasia's Commons category is recorded as Craniofrontonasal dysplasia[9].
- craniofrontonasal dysplasia's health specialty is recorded as medical genetics[10].
- craniofrontonasal dysplasia's genetic association is recorded as EFNB1[11].
- craniofrontonasal dysplasia's exact match is recorded as http://purl.obolibrary.org/obo/DOID_14737[12].
- craniofrontonasal dysplasia's exact match is recorded as http://identifiers.org/doid/DOID:14737[13].
- craniofrontonasal dysplasia's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1520[14].
- craniofrontonasal dysplasia's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
Why It Matters
craniofrontonasal dysplasia draws 148 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #83 of 308).[2] It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[16] It is known by 4 alternative names across languages and contexts.[17]