Armfield Syndrome (MRXSA)

Alias:

X-Linked Intellectual Disability, Armfield Type

Mental Retardation Syndrome, X-Linked, Armfield Type

Syndromic X-Linked Mental Retardation Armfield Type

Armfield X-Linked Mental Retardation Syndrome

Mrxsa

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Armfield Syndrome, also known as x-linked intellectual disability, armfield type, is related to intellectual developmental disorder, x-linked, syndromic, armfield type and mandibulofacial dysostosis, guion-almeida type, and has symptoms including seizures An important gene associated with Armfield Syndrome is FAM50A (Family With Sequence Similarity 50 Member A). Affiliated tissues include eye, and related phenotypes are seizure and global developmental delay

Related ID：

MALACARDS：ARM005