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intellectual disability, autosomal dominant 47 | RareConnect | RareConnect.io

/congenital nervous system disorder

/multiple congenital anomalies/dysmorphic syndrome-intellectual disability

/autosomal dominant non-syndromic intellectual disability

/intellectual disability, autosomal dominant 47

intellectual disability, autosomal dominant 47

Rare Disease

MONDO:0030912

Also Known As

STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndromeintellectual disability, autosomal dominant 47MRD47autosomal dominant intellectual disability 47autosomal dominant mental retardation 47mental retardation, autosomal dominant 47

Patient-Friendly Information

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Associated Genes

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:617635 ↗

Orphanet

Orphanet:502434 ↗

GARD

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