Cebalid Syndrome (CEBALID)

Alias:

Mn1 C-Terminal Truncation Syndrome

Craniofacial Defects, Dysmorphic Ears, Structural Brain Abnormalities, Expressive Language Delay, and Impaired Intellectual Development

Cebalid

Mctt

Mn1 C-Terminal Truncation Syndrome

Mctt Syndrome

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Cebalid Syndrome, also known as mn1 c-terminal truncation syndrome, is related to leukemia, acute myeloid and rhombencephalosynapsis. An important gene associated with Cebalid Syndrome is MN1 (MN1 Proto-Oncogene, Transcriptional Regulator). Affiliated tissues include brain and cerebellum, and related phenotypes are short nose and thick eyebrow

Related ID：

MALACARDS：CBL011

OMIM：618774

MESH：D008607