MEHMO syndrome

Summary

MEHMO syndrome is a developmental defect during embryogenesis^[1]. It is known by 15 alternative names across languages and contexts.^[2]

Key Facts

• MEHMO syndrome's instance of is recorded as developmental defect during embryogenesis^[3].
• MEHMO syndrome's instance of is recorded as class of disease^[4].
• MEHMO syndrome is a type of X-linked intellectual disability^[5].
• MEHMO syndrome is a type of mitochondrial disease with epilepsy^[6].
• MEHMO syndrome is a type of mitochondrial disease with peripheral neuropathy^[7].
• MEHMO syndrome is a type of syndromic obesity^[8].
• MEHMO syndrome is a type of X-linked recessive disease^[9].
• MEHMO syndrome's health specialty is recorded as medical genetics^[10].
• MEHMO syndrome's genetic association is recorded as EIF2S3^[11].
• MEHMO syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060801^[12].
• MEHMO syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060801^[13].
• MEHMO syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_85282^[14].
• MEHMO syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine^[15].

Why It Matters

MEHMO syndrome is known by 15 alternative names across languages and contexts.^[2]