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Ontology Browser

Term:
autosomal dominant intellectual developmental disorder 10 (DOID:0070040)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1) Naked Mole-rat: (1) Green Monkey: (1)
Parent Terms Term With Siblings Child Terms
Arboleda-Tham syndrome  
autosomal dominant intellectual developmental disorder 1  
autosomal dominant intellectual developmental disorder 10  
An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the CACNG2 gene on chromosome 22q12.3. (DO)
autosomal dominant intellectual developmental disorder 11  
autosomal dominant intellectual developmental disorder 13  
autosomal dominant intellectual developmental disorder 19  
autosomal dominant intellectual developmental disorder 2  
autosomal dominant intellectual developmental disorder 21  
autosomal dominant intellectual developmental disorder 22  
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autosomal dominant intellectual developmental disorder 3  
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autosomal dominant intellectual developmental disorder 34  
autosomal dominant intellectual developmental disorder 35  
autosomal dominant intellectual developmental disorder 36  
autosomal dominant intellectual developmental disorder 38  
autosomal dominant intellectual developmental disorder 39  
autosomal dominant intellectual developmental disorder 4  
autosomal dominant intellectual developmental disorder 40  
autosomal dominant intellectual developmental disorder 41  
autosomal dominant intellectual developmental disorder 42  
autosomal dominant intellectual developmental disorder 43  
autosomal dominant intellectual developmental disorder 44  
autosomal dominant intellectual developmental disorder 45  
autosomal dominant intellectual developmental disorder 46  
autosomal dominant intellectual developmental disorder 47  
autosomal dominant intellectual developmental disorder 48  
autosomal dominant intellectual developmental disorder 5  
autosomal dominant intellectual developmental disorder 50  
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autosomal dominant intellectual developmental disorder 52  
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Autosomal Dominant Intellectual Developmental Disorder 57  
Autosomal Dominant Intellectual Developmental Disorder 58  
Autosomal Dominant Intellectual Developmental Disorder 59  
autosomal dominant intellectual developmental disorder 6  
Autosomal Dominant Intellectual Developmental Disorder 60  
Autosomal Dominant Intellectual Developmental Disorder 61  
Autosomal Dominant Intellectual Developmental Disorder 62  
Autosomal Dominant Intellectual Developmental Disorder 63 with Macrocephaly  
Autosomal Dominant Intellectual Developmental Disorder 64  
Autosomal Dominant Intellectual Developmental Disorder 65  
Autosomal Dominant Intellectual Developmental Disorder 66  
Autosomal Dominant Intellectual Developmental Disorder 67  
Autosomal Dominant Intellectual Developmental Disorder 68  
Autosomal Dominant Intellectual Developmental Disorder 69  
autosomal dominant intellectual developmental disorder 7  
Autosomal Dominant Intellectual Developmental Disorder 70  
Autosomal Dominant Intellectual Developmental Disorder 71  
Autosomal Dominant Intellectual Developmental Disorder 72  
Autosomal Dominant Intellectual Developmental Disorder 73  
Autosomal Dominant Intellectual Developmental Disorder 74  
autosomal dominant intellectual developmental disorder 8  
Clark-Baraitser syndrome  
Coffin-Siris syndrome +   
Coffin-Siris syndrome 9  
developmental delay, dysmorphic facies, and brain anomalies  
developmental delay, hypotonia, and impaired language  
GAND syndrome  
Helsmoortel-Van Der Aa syndrome  
intellectual developmental disorder with autistic features and language delay, with or without seizures  
intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies  
Koolen de Vries syndrome  
Luo-Schoch-Yamamoto syndrome  
NESCAV syndrome  
neurodevelopmental disorder with dysmorphic facies and behavioral abnormalities  
neurodevelopmental disorder with dysmorphic facies and distal limb anomalies  
neurodevelopmental disorder with dysmorphic facies and thin corpus callosum  
neurodevelopmental disorder with eye movement abnormalities and ataxia  
neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures  
neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language  
neurodevelopmental disorder with speech impairment and dysmorphic facies  
Pierpont syndrome  
Schuurs-Hoeijmakers syndrome  
Sifrim-Hitz-Weiss syndrome  
Vulto-van Silfout-de Vries syndrome  
White-Sutton syndrome  
Xia-Gibbs syndrome  

Synonyms
Exact Synonyms: INTELLECTUAL DISABILITY, AUTOSOMAL DOMINANT 10 ;   MRD10 ;   autosomal dominant mental retardation 10 ;   autosomal dominant non-syndromic intellectual disability 10
Primary IDs: OMIM:614256
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/21376300 "DO" "DO"

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