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Disease association ontology term - MONDO:0015160 - multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome

Term summary

ID
MONDO:0015160
Name
multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome
Ontology or CV name
Disease association

Parents

Annotation

Disease association

MONDO:0008726 - Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis

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Genes:

MONDO:0007301 - cerebrocostomandibular syndrome

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MONDO:0016817 - Meier-Gorlin syndrome

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MONDO:0009143 - Meier-Gorlin syndrome 1

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MONDO:0013428 - Meier-Gorlin syndrome 2

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MONDO:0013430 - Meier-Gorlin syndrome 3

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MONDO:0013431 - Meier-Gorlin syndrome 4

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MONDO:0013432 - Meier-Gorlin syndrome 5

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MONDO:0014894 - Meier-Gorlin syndrome 7

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MONDO:0033046 - Meier-Gorlin syndrome 8

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MONDO:0980992 - Meier-Gorlin syndrome 9

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MONDO:0054593 - microcephaly 18, primary, autosomal dominant

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MONDO:0018997 - Noonan syndrome

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MONDO:0033669 - Noonan syndrome 13

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MONDO:0012371 - Noonan syndrome 3

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MONDO:0013186 - Noonan syndrome 6

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MONDO:0054588 - Noonan syndrome-like disorder with loose anagen hair 2

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MONDO:0010572 - occipital horn syndrome

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MONDO:0800042 - restrictive dermopathy 1

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MONDO:0044634 - retinitis pigmentosa-hearing loss-premature aging-short stature-facial dysmorphism syndrome

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MONDO:0014848 - TELO2-related intellectual disability-neurodevelopmental disorder

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