Miller syndrome

Summary

Miller syndrome is a head and neck disease^[1].

Key Facts

• Miller syndrome's instance of is recorded as head and neck disease^[2].
• Miller syndrome's instance of is recorded as developmental defect during embryogenesis^[3].
• Miller syndrome's instance of is recorded as rare disease^[4].
• Miller syndrome's instance of is recorded as class of disease^[5].
• Miller syndrome is a type of acrofacial dysostosis^[6].
• Miller syndrome is a type of secondary ectropion^[7].
• Miller syndrome is a type of syndromic palpebral coloboma^[8].
• Miller syndrome is a type of multiple congenital anomalies/dysmorphic syndrome without intellectual disability^[9].
• Miller syndrome is a type of syndromic developmental defect of the eye^[10].
• Miller syndrome is a type of branchial arch or oral-acral syndrome^[11].
• Miller syndrome is a type of syndrome or malformation associated with head and neck malformations^[12].
• Miller syndrome is a type of autosomal recessive disease^[13].
• Miller syndrome is a type of syndrome^[14].
• Miller syndrome's Commons category is recorded as Miller syndrome^[15].
• Miller syndrome's ICD-9-CM is recorded as 759.89^[16].
• Miller syndrome's genetic association is recorded as DHODH^[17].
• Miller syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111259^[18].
• Miller syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0111259^[19].
• Miller syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine^[20].