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Disease association ontology term - MONDO:0100601 - autosomal dominant syndromic intellectual disability

Term summary

ID
MONDO:0100601
Name
autosomal dominant syndromic intellectual disability
Ontology or CV name
Disease association
Definition
Autosomal dominant form of syndromic intellectual disability.

Parents

Annotation

Disease association

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

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Genes:

MONDO:0013578 - DYRK1A-related intellectual disability syndrome

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Genes:

MONDO:0014602 - Houge-Janssens syndrome 1

References:

Genes:

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

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Genes:

MONDO:0013805 - intellectual disability, autosomal dominant 13

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Genes:

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

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Genes:

MONDO:0011213 - Pierpont syndrome

References:

Genes: