PomBase home

Disease association ontology term - MONDO:0019181 - non-syndromic X-linked intellectual disability

Term summary

ID
MONDO:0019181
Name
non-syndromic X-linked intellectual disability
Ontology or CV name
Disease association
Definition
Nonspecific X-linked intellectual deficiencies (MRX) belong to the family of sex-linked intellectual deficiencies (XLMR). In contrast to syndromic or specific X-linked intellectual deficiencies (MRXS), which also present with associated physical, neurological and/or psychiatric manifestations, intellectual deficiency is the only symptom of MRX.

Parents

Annotation

Disease association

MONDO:0019181 - non-syndromic X-linked intellectual disability

References:

Genes:

MONDO:0010659 - FRAXE intellectual disability

References:

Genes:

MONDO:0026723 - intellectual developmental disorder, X-linked 108

References:

Genes:

MONDO:0958200 - intellectual developmental disorder, X-linked 113

References:

Genes:

MONDO:0975828 - intellectual developmental disorder, X-linked 114

References:

Genes:

MONDO:0010497 - intellectual disability, X-linked 102

References:

Genes:

MONDO:0049222 - intellectual disability, X-linked 107

References:

Genes:

MONDO:0010447 - intellectual disability, X-linked 19

References:

Genes:

MONDO:0010361 - intellectual disability, X-linked 30

References:

Genes:

MONDO:0010451 - intellectual disability, X-linked 41

References:

Genes:

MONDO:0010313 - intellectual disability, X-linked 63

References:

Genes:

MONDO:0010660 - intellectual disability, X-linked 9

References:

Genes: