agnathia-otocephaly complex
Human disease
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agnathia-otocephaly complex
Summary
agnathia-otocephaly complex is a developmental defect during embryogenesis[1]. It has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- agnathia-otocephaly complex's instance of is recorded as developmental defect during embryogenesis[3].
- agnathia-otocephaly complex's instance of is recorded as rare disease[4].
- agnathia-otocephaly complex's instance of is recorded as class of disease[5].
- agnathia-otocephaly complex is a type of congenital disorder[6].
- agnathia-otocephaly complex is a type of genetic syndromic intellectual disability[7].
- agnathia-otocephaly complex is a type of multiple congenital anomalies/dysmorphic syndrome-intellectual disability[8].
- agnathia-otocephaly complex is a type of disease[9].
- agnathia-otocephaly complex's Commons category is recorded as Otocephaly[10].
- agnathia-otocephaly complex's ICD-9-CM is recorded as 759.89[11].
- agnathia-otocephaly complex's health specialty is recorded as medical genetics[12].
- agnathia-otocephaly complex's genetic association is recorded as PRRX1[13].
- agnathia-otocephaly complex's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060341[14].
- agnathia-otocephaly complex's exact match is recorded as http://identifiers.org/doid/DOID:0060341[15].
- agnathia-otocephaly complex's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_990[16].
- agnathia-otocephaly complex's on focus list of Wikimedia project is recorded as WikiProject Medicine[17].
Why It Matters
agnathia-otocephaly complex has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[2] It is known by 8 alternative names across languages and contexts.[18]