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Disease association ontology term - MONDO:0000509 - non-syndromic intellectual disability

Term summary

ID
MONDO:0000509
Name
non-syndromic intellectual disability
Ontology or CV name
Disease association
Definition
An intellectual disability that is not part of a larger syndrome.

Parents

Annotation

Disease association

MONDO:0100255 - adenosine kinase deficiency

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Genes:

MONDO:0014648 - Al-Raqad syndrome

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Genes:

MONDO:0019502 - autosomal recessive non-syndromic intellectual disability

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Genes:

MONDO:0030914 - Clark-Baraitser syndrome

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MONDO:0010659 - FRAXE intellectual disability

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Genes:

MONDO:0040500 - glycosylphosphatidylinositol biosynthesis defect 16

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Genes:

MONDO:0032823 - intellectual developmental disorder 60 with seizures

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MONDO:0032485 - intellectual developmental disorder 61

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MONDO:0957536 - intellectual developmental disorder, autosomal dominant 73

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MONDO:0032662 - intellectual developmental disorder, autosomal recessive 67

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MONDO:0032665 - intellectual developmental disorder, autosomal recessive 68

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MONDO:0032789 - intellectual developmental disorder, autosomal recessive 71

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MONDO:0030533 - intellectual developmental disorder, autosomal recessive 73

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MONDO:0957288 - intellectual developmental disorder, autosomal recessive 79

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MONDO:0958204 - intellectual developmental disorder, autosomal recessive 81

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

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

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

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MONDO:0014580 - intellectual disability, autosomal dominant 33

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MONDO:0014842 - intellectual disability, autosomal dominant 41

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MONDO:0030912 - intellectual disability, autosomal dominant 47

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MONDO:0030916 - intellectual disability, autosomal dominant 50

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MONDO:0030917 - intellectual disability, autosomal dominant 51

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MONDO:0030921 - intellectual disability, autosomal dominant 55, with seizures

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MONDO:0030922 - intellectual disability, autosomal dominant 56

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MONDO:0020847 - intellectual disability, autosomal dominant 58

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MONDO:0013173 - intellectual disability, autosomal recessive 13

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MONDO:0013528 - intellectual disability, autosomal recessive 14

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MONDO:0014348 - intellectual disability, autosomal recessive 42

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MONDO:0014409 - intellectual disability, autosomal recessive 44

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MONDO:0012613 - intellectual disability, autosomal recessive 5

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MONDO:0014649 - intellectual disability, autosomal recessive 50

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Genes:

MONDO:0014815 - intellectual disability, autosomal recessive 52

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MONDO:0014930 - intellectual disability, autosomal recessive 56

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Genes:

MONDO:0014996 - intellectual disability, autosomal recessive 58

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MONDO:0015020 - intellectual disability, autosomal recessive 59

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MONDO:0044313 - intellectual disability, autosomal recessive 60

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MONDO:0020850 - intellectual disability, autosomal recessive 65

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Genes:

MONDO:0012615 - intellectual disability, autosomal recessive 7

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Genes:

MONDO:0010497 - intellectual disability, X-linked 102

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MONDO:0049222 - intellectual disability, X-linked 107

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MONDO:0010447 - intellectual disability, X-linked 19

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MONDO:0010361 - intellectual disability, X-linked 30

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MONDO:0010451 - intellectual disability, X-linked 41

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MONDO:0010313 - intellectual disability, X-linked 63

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MONDO:0010660 - intellectual disability, X-linked 9

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Genes:

MONDO:0013266 - neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language

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

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MONDO:0016396 - pontocerebellar hypoplasia type 1

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MONDO:0013853 - pontocerebellar hypoplasia type 1B

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MONDO:0014485 - pontocerebellar hypoplasia, type 1C

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Genes:

MONDO:0013624 - Rafiq syndrome

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