MRT31
MCID: MNT160
MIFTS: 13
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Mental Retardation, Autosomal Recessive 31 (MRT31)
Categories:
Ear diseases, Eye diseases, Fetal diseases, Gastrointestinal diseases, Genetic diseases, Mental diseases, Metabolic diseases, Neuronal diseases, Rare diseases
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MalaCards integrated aliases for Mental Retardation, Autosomal Recessive 31:
Characteristics:OMIM®:57 (Updated 05-Mar-2021)
Inheritance:
autosomal recessive
Miscellaneous:
one family reported (last curated november 2011) HPO:31Classifications:
MalaCards categories:
Global: Genetic diseases Metabolic diseases Fetal diseases Rare diseases Anatomical: Neuronal diseases Eye diseases Mental diseases Gastrointestinal diseases Ear diseases |
MalaCards based summary :
Mental Retardation, Autosomal Recessive 31, is also known as mrt31. An important gene associated with Mental Retardation, Autosomal Recessive 31 is MRT31 (Mental Retardation, Autosomal Recessive 31). Related phenotype is intellectual disability.
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Human phenotypes related to Mental Retardation, Autosomal Recessive 31:31
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Articles related to Mental Retardation, Autosomal Recessive 31:
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GEO
for disease gene expression data for Mental Retardation, Autosomal Recessive 31.
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