MEND syndrome
human disease
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MEND syndrome
Summary
MEND syndrome is a developmental defect during embryogenesis[1]. It is known by 10 alternative names across languages and contexts.[2]
Key Facts
- MEND syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- MEND syndrome's instance of is recorded as rare disease[4].
- MEND syndrome's instance of is recorded as class of disease[5].
- MEND syndrome is a type of genetic syndromic intellectual disability[6].
- MEND syndrome is a type of sterol biosynthesis disorder[7].
- MEND syndrome is a type of rare genetic developmental defect during embryogenesis[8].
- MEND syndrome is a type of syndromic dyslipidemia[9].
- MEND syndrome is a type of X-linked recessive disease[10].
- MEND syndrome is a type of lipid metabolism disorder[11].
- MEND syndrome's genetic association is recorded as EBP[12].
- MEND syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_401973[13].
- MEND syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111865[14].
- MEND syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0111865[15].
Why It Matters
MEND syndrome is known by 10 alternative names across languages and contexts.[2]