Ayme-Gripp syndrome
human disease
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Summary
Ayme-Gripp syndrome is a head and neck disease[1]. It is known by 5 alternative names across languages and contexts.[2]
Key Facts
- Instance of: developmental defect during embryogenesis[3], rare disease[4], class of disease[5]
- Subclass of: syndromic genetic deafness[6], syndromic cataract[7], multiple congenital anomalies/dysmorphic syndrome-intellectual disability[8], genetic syndromic intellectual disability[9], syndrome[10], autosomal dominant disease[11]
- Genetic association: MAF[12]
- Exact match: http://www.orpha.net/ORDO/Orphanet_477668[13], http://purl.obolibrary.org/obo/DOID_0111688[14], http://identifiers.org/doid/DOID:0111688[15]