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Disease association ontology term - MONDO:0100284 - X-linked intellectual disability

Term summary

ID
MONDO:0100284
Name
X-linked intellectual disability
Ontology or CV name
Disease association
Definition
An X-linked intellectual deficiency in which not enough information is known, reported or published to indicate whether a gene causes non-syndromic or syndromic presentations.

Parents

Annotation

Disease association

MONDO:0010477 - blepharophimosis - intellectual disability syndrome, MKB type

References:

Genes:

MONDO:0010561 - Coffin-Lowry syndrome

References:

Genes:

MONDO:0010333 - corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome

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Genes:

MONDO:0010590 - FG syndrome 1

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Genes:

MONDO:0010659 - FRAXE intellectual disability

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Genes:

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

References:

Genes:

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

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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:0010250 - intellectual disability, X-linked 49

References:

Genes:

MONDO:0010313 - intellectual disability, X-linked 63

References:

Genes:

MONDO:0010660 - intellectual disability, X-linked 9

References:

Genes:

MONDO:0010407 - intellectual disability, X-linked syndromic, Turner type

References:

Genes:

MONDO:0010500 - intellectual disability, X-linked, syndromic 33

References:

Genes:

MONDO:0030908 - intellectual disability, X-linked, syndromic, 35

References:

Genes:

MONDO:0030909 - intellectual disability, X-linked, syndromic, Houge type

References:

Genes:

MONDO:0010258 - MEHMO syndrome

References:

Genes:

MONDO:0010671 - microphthalmia, syndromic 1

References:

Genes:

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

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Genes:

MONDO:0010457 - Ogden syndrome

References:

Genes:

MONDO:0010398 - syndromic X-linked intellectual disability 14

References:

Genes:

MONDO:0010574 - syndromic X-linked intellectual disability 5

References:

Genes:

MONDO:0010355 - syndromic X-linked intellectual disability Claes-Jensen type

References:

Genes:

MONDO:0010461 - syndromic X-linked intellectual disability Nascimento type

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Genes:

MONDO:0010286 - syndromic X-linked intellectual disability Siderius type

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Genes:

MONDO:0010665 - Wilson-Turner syndrome

References:

Genes:

MONDO:0010655 - X-linked intellectual disability with marfanoid habitus

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Genes:

MONDO:0010306 - X-linked intellectual disability, Cabezas type

References:

Genes:

MONDO:0015601 - X-linked intellectual disability, van Esch type

References:

Genes:

MONDO:0010496 - X-linked intellectual disability-short stature-overweight syndrome

References:

Genes: