Intellectual disability, autosomal dominant 53
- Synonyms
- INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 53; MENTAL RETARDATION, AUTOSOMAL DOMINANT 53
Available tests
Clinical tests (4 available)
Clinical features
Help- Abnormality of head or neck
- Downslanted palpebral fissures
Downslanted palpebral fissures
- MedGen UID: 98391
- Concept ID: C0423110
- Finding: Finding
Abnormality of head or neck
- Epicanthus
Epicanthus
- MedGen UID: 151862
- Concept ID: C0678230
- Finding: Congenital Abnormality
Abnormality of head or neck
- Wide mouth
Wide mouth
- MedGen UID: 44238
- Concept ID: C0024433
- Finding: Congenital Abnormality
Abnormality of head or neck
- Downslanted palpebral fissures
- Abnormality of limbs
- Genu valgum
Genu valgum
- MedGen UID: 154364
- Concept ID: C0576093
- Finding: Anatomical Abnormality
Abnormality of limbs
- Short femur
Short femur
- MedGen UID: 87499
- Concept ID: C0345375
- Finding: Congenital Abnormality
Abnormality of limbs
- Genu valgum
- Abnormality of the cardiovascular system
- Ventricular septal defect
Ventricular septal defect
- MedGen UID: 42366
- Concept ID: C0018818
- Finding: Congenital Abnormality
Abnormality of the cardiovascular system
- Ventricular septal defect
- Abnormality of the digestive system
- Duodenal atresia
Duodenal atresia
- MedGen UID: 75602
- Concept ID: C0266174
- Finding: Congenital Abnormality
Abnormality of the digestive system
- Gastrointestinal dysmotility
Gastrointestinal dysmotility
- MedGen UID: 324638
- Concept ID: C1836923
- Finding: Finding
Abnormality of the digestive system
- Intestinal malrotation
Intestinal malrotation
- MedGen UID: 113153
- Concept ID: C0221210
- Finding: Congenital Abnormality
Abnormality of the digestive system
- Duodenal atresia
- Abnormality of the eye
- Hypotelorism
Hypotelorism
- MedGen UID: 96107
- Concept ID: C0424711
- Finding: Finding
Abnormality of the eye
- Strabismus
Strabismus
- MedGen UID: 21337
- Concept ID: C0038379
- Finding: Disease or Syndrome
Abnormality of the eye
- Visual impairment
Visual impairment
- MedGen UID: 777085
- Concept ID: C3665347
- Finding: Finding
Abnormality of the eye
- Hypotelorism
- Abnormality of the genitourinary system
- Cryptorchidism
Cryptorchidism
- MedGen UID: 8192
- Concept ID: C0010417
- Finding: Congenital Abnormality
Abnormality of the genitourinary system
- Hydronephrosis
Hydronephrosis
- MedGen UID: 42531
- Concept ID: C0020295
- Finding: Disease or Syndrome
Abnormality of the genitourinary system
- Micropenis
Micropenis
- MedGen UID: 1633603
- Concept ID: C4551492
- Finding: Congenital Abnormality
Abnormality of the genitourinary system
- Cryptorchidism
- Abnormality of the integument
- Blue nevus
Blue nevus
- MedGen UID: 104930
- Concept ID: C0206736
- Finding: Neoplastic Process
Abnormality of the integument
- Frontal upsweep of hair
Frontal upsweep of hair
- MedGen UID: 452910
- Concept ID: C1185616
- Finding: Finding
Abnormality of the integument
- Blue nevus
- Abnormality of the musculoskeletal system
- Brachycephaly
Brachycephaly
- MedGen UID: 113165
- Concept ID: C0221356
- Finding: Congenital Abnormality
Abnormality of the musculoskeletal system
- Hypotonia
Hypotonia
- MedGen UID: 10133
- Concept ID: C0026827
- Finding: Finding
Abnormality of the musculoskeletal system
- Infantile axial hypotonia
Infantile axial hypotonia
- MedGen UID: 812934
- Concept ID: C3806604
- Finding: Finding
Abnormality of the musculoskeletal system
- Joint hypermobility
Joint hypermobility
- MedGen UID: 336793
- Concept ID: C1844820
- Finding: Finding
Abnormality of the musculoskeletal system
- Macrocephaly
Macrocephaly
- MedGen UID: 745757
- Concept ID: C2243051
- Finding: Finding
Abnormality of the musculoskeletal system
- Microcephaly
Microcephaly
- MedGen UID: 1644158
- Concept ID: C4551563
- Finding: Finding
Abnormality of the musculoskeletal system
- Posterior plagiocephaly
Posterior plagiocephaly
- MedGen UID: 892298
- Concept ID: C4021160
- Finding: Anatomical Abnormality
Abnormality of the musculoskeletal system
- Brachycephaly
- Abnormality of the nervous system
- Absent speech
Absent speech
- MedGen UID: 340737
- Concept ID: C1854882
- Finding: Finding
Abnormality of the nervous system
- Bilateral tonic-clonic seizure
Bilateral tonic-clonic seizure
- MedGen UID: 141670
- Concept ID: C0494475
- Finding: Sign or Symptom
Abnormality of the nervous system
- Circadian rhythm sleep disorder
Circadian rhythm sleep disorder
- MedGen UID: 167920
- Concept ID: C0877792
- Finding: Pathologic Function
Abnormality of the nervous system
- Delayed ability to walk
Delayed ability to walk
- MedGen UID: 66034
- Concept ID: C0241726
- Finding: Finding
Abnormality of the nervous system
- Delayed gross motor development
Delayed gross motor development
- MedGen UID: 332508
- Concept ID: C1837658
- Finding: Finding
Abnormality of the nervous system
- Delayed speech and language development
Delayed speech and language development
- MedGen UID: 105318
- Concept ID: C0454644
- Finding: Finding
Abnormality of the nervous system
- EEG abnormality
EEG abnormality
- MedGen UID: 56235
- Concept ID: C0151611
- Finding: Finding
Abnormality of the nervous system
- Febrile seizure (within the age range of 3 months to 6 years)
Febrile seizure (within the age range of 3 months to 6 years)
- MedGen UID: 3232
- Concept ID: C0009952
- Finding: Disease or Syndrome
Abnormality of the nervous system
- Generalized non-motor (absence) seizure
Generalized non-motor (absence) seizure
- MedGen UID: 1385688
- Concept ID: C4316903
- Finding: Disease or Syndrome
Abnormality of the nervous system
- Global developmental delay
Global developmental delay
- MedGen UID: 107838
- Concept ID: C0557874
- Finding: Finding
Abnormality of the nervous system
- Hyperintensity of cerebral white matter on MRI
Hyperintensity of cerebral white matter on MRI
- MedGen UID: 811125
- Concept ID: C2938912
- Finding: Pathologic Function
Abnormality of the nervous system
- Intellectual disability
Intellectual disability
- MedGen UID: 811461
- Concept ID: C3714756
- Finding: Mental or Behavioral Dysfunction
Abnormality of the nervous system
- Involuntary movements
Involuntary movements
- MedGen UID: 140884
- Concept ID: C0427086
- Finding: Sign or Symptom
Abnormality of the nervous system
- Irritability
Irritability
- MedGen UID: 397841
- Concept ID: C2700617
- Finding: Mental Process
Abnormality of the nervous system
- Thick corpus callosum
Thick corpus callosum
- MedGen UID: 371993
- Concept ID: C1835194
- Finding: Finding
Abnormality of the nervous system
- Unsteady gait
Unsteady gait
- MedGen UID: 68544
- Concept ID: C0231686
- Finding: Finding
Abnormality of the nervous system
- Absent speech
- Ear malformation
- Microtia
Microtia
- MedGen UID: 57535
- Concept ID: C0152423
- Finding: Congenital Abnormality
Ear malformation
- Microtia
- Growth abnormality
- Growth delay
Growth delay
- MedGen UID: 99124
- Concept ID: C0456070
- Finding: Pathologic Function
Growth abnormality
- Overgrowth
Overgrowth
- MedGen UID: 376550
- Concept ID: C1849265
- Finding: Finding
Growth abnormality
- Growth delay
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