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Disease association ontology term - MONDO:0019502 - autosomal recessive non-syndromic intellectual disability

Term summary

ID
MONDO:0019502
Name
autosomal recessive non-syndromic intellectual disability
Ontology or CV name
Disease association
Definition
Autosomal recessive form of non-syndromic intellectual disability.

Parents

Annotation

Disease association

MONDO:0019502 - autosomal recessive non-syndromic 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:0040500 - glycosylphosphatidylinositol biosynthesis defect 16

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Genes:

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: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: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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Genes:

MONDO:0012615 - intellectual disability, autosomal recessive 7

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MONDO:0016396 - pontocerebellar hypoplasia type 1

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Genes:

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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