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Disease association ontology term - MONDO:0001071 - intellectual disability

Term summary

ID
MONDO:0001071
Name
intellectual disability
Ontology or CV name
Disease association
Definition
A broad category of disorders characterized by an impairment to the intelligence an individual possesses. These impairments can result from trauma, birth, or disease and are not restricted to any particular age group.

Parents

Annotation

Disease association

MONDO:0001071 - intellectual disability

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Genes:

MONDO:0100255 - adenosine kinase deficiency

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Genes:

MONDO:0014648 - Al-Raqad syndrome

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Genes:

MONDO:0014558 - autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome

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MONDO:0019502 - autosomal recessive non-syndromic intellectual disability

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

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MONDO:0013644 - Charcot-Marie-Tooth disease axonal type 2O

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MONDO:0010441 - CK syndrome

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MONDO:0030914 - Clark-Baraitser syndrome

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MONDO:0010561 - Coffin-Lowry syndrome

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

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MONDO:0013578 - DYRK1A-related intellectual disability syndrome

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MONDO:0010590 - FG syndrome 1

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MONDO:0010659 - FRAXE intellectual disability

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MONDO:0040500 - glycosylphosphatidylinositol biosynthesis defect 16

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MONDO:0014602 - Houge-Janssens syndrome 1

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MONDO:0032823 - intellectual developmental disorder 60 with seizures

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MONDO:0032485 - intellectual developmental disorder 61

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MONDO:0015022 - intellectual developmental disorder with dysmorphic facies and ptosis

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MONDO:0044319 - intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies

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MONDO:0976124 - intellectual developmental disorder with polymicrogyria and seizures

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MONDO:0023657 - intellectual developmental disorder, autosomal dominant 65

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MONDO:0030891 - intellectual developmental disorder, autosomal dominant 66

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MONDO:0029465 - intellectual developmental disorder, autosomal dominant 69

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MONDO:0859333 - intellectual developmental disorder, autosomal dominant 70

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Genes:

MONDO:0957397 - intellectual developmental disorder, autosomal dominant 72

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MONDO:0957536 - intellectual developmental disorder, autosomal dominant 73

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MONDO:0958203 - intellectual developmental disorder, autosomal dominant 74

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MONDO:0979575 - intellectual developmental disorder, autosomal dominant 76

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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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Genes:

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

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Genes:

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

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Genes:

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

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Genes:

MONDO:0013805 - intellectual disability, autosomal dominant 13

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MONDO:0014580 - intellectual disability, autosomal dominant 33

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MONDO:0014617 - intellectual disability, autosomal dominant 38

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MONDO:0014842 - intellectual disability, autosomal dominant 41

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MONDO:0014855 - intellectual disability, autosomal dominant 42

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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:0013656 - intellectual disability, autosomal dominant 9

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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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MONDO:0014815 - intellectual disability, autosomal recessive 52

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MONDO:0014832 - intellectual disability, autosomal recessive 53

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MONDO:0014930 - intellectual disability, autosomal recessive 56

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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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MONDO:0012615 - intellectual disability, autosomal recessive 7

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MONDO:0010497 - intellectual disability, X-linked 102

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MONDO:0049222 - intellectual disability, X-linked 107

References:

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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:

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MONDO:0010250 - intellectual disability, X-linked 49

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

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

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

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Genes:

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

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Genes:

MONDO:0011053 - intellectual disability-sparse hair-brachydactyly syndrome

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Genes:

MONDO:0010258 - MEHMO syndrome

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Genes:

MONDO:0010671 - microphthalmia, syndromic 1

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Genes:

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

References:

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

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MONDO:0010457 - Ogden syndrome

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MONDO:0011213 - Pierpont syndrome

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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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MONDO:0013624 - Rafiq syndrome

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MONDO:0010398 - syndromic X-linked intellectual disability 14

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MONDO:0010574 - syndromic X-linked intellectual disability 5

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

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

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

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MONDO:0010665 - Wilson-Turner syndrome

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

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

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

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

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