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Disease association ontology term - MONDO:0020119 - X-linked syndromic intellectual disability

Term summary

ID
MONDO:0020119
Name
X-linked syndromic intellectual disability
Ontology or CV name
Disease association
Definition
A syndromic intellectual disability with an X-linked mode of inheritance.

Parents

Annotation

Disease association

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

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Genes:

MONDO:0010561 - Coffin-Lowry syndrome

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Genes:

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

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MONDO:0010590 - FG syndrome 1

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MONDO:0010250 - intellectual disability, X-linked 49

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

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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:0010457 - Ogden 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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