Microcephaly 20, primary, autosomal recessive
Available tests
Clinical tests (8 available)
Clinical features
Help- Abnormality of head or neck
- Sloping forehead
Sloping forehead
- MedGen UID: 346640
- Concept ID: C1857679
- Finding: Finding
Abnormality of head or neck
- Sloping forehead
- Abnormality of the eye
- Blindness
Blindness
- MedGen UID: 99138
- Concept ID: C0456909
- Finding: Disease or Syndrome
Abnormality of the eye
- Microphthalmia
Microphthalmia
- MedGen UID: 10033
- Concept ID: C0026010
- Finding: Congenital Abnormality
Abnormality of the eye
- Optic nerve hypoplasia
Optic nerve hypoplasia
- MedGen UID: 137901
- Concept ID: C0338502
- Finding: Disease or Syndrome
Abnormality of the eye
- Strabismus
Strabismus
- MedGen UID: 21337
- Concept ID: C0038379
- Finding: Disease or Syndrome
Abnormality of the eye
- Blindness
- Abnormality of the genitourinary system
- Bilateral renal agenesis
Bilateral renal agenesis
- MedGen UID: 296299
- Concept ID: C1609433
- Finding: Disease or Syndrome
Abnormality of the genitourinary system
- Hyperechogenic kidneys
Hyperechogenic kidneys
- MedGen UID: 477530
- Concept ID: C3275899
- Finding: Finding
Abnormality of the genitourinary system
- Renal hypoplasia
Renal hypoplasia
- MedGen UID: 120571
- Concept ID: C0266295
- Finding: Congenital Abnormality
Abnormality of the genitourinary system
- Ureteral agenesis
Ureteral agenesis
- MedGen UID: 868560
- Concept ID: C4022959
- Finding: Finding
Abnormality of the genitourinary system
- Uterine hypoplasia
Uterine hypoplasia
- MedGen UID: 120575
- Concept ID: C0266399
- Finding: Congenital Abnormality
Abnormality of the genitourinary system
- Vaginal atresia
Vaginal atresia
- MedGen UID: 232948
- Concept ID: C1321884
- Finding: Congenital Abnormality
Abnormality of the genitourinary system
- Bilateral renal agenesis
- Abnormality of the musculoskeletal system
- Generalized hypotonia
Generalized hypotonia
- MedGen UID: 346841
- Concept ID: C1858120
- Finding: Finding
Abnormality of the musculoskeletal system
- Microcephaly
Microcephaly
- MedGen UID: 1644158
- Concept ID: C4551563
- Finding: Finding
Abnormality of the musculoskeletal system
- Generalized hypotonia
- Abnormality of the nervous system
- Arrhinencephaly
Arrhinencephaly
- MedGen UID: 36258
- Concept ID: C0078982
- Finding: Congenital Abnormality
Abnormality of the nervous system
- Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder
- MedGen UID: 220387
- Concept ID: C1263846
- Finding: Mental or Behavioral Dysfunction
Abnormality of the nervous system
- Cerebellar hypoplasia
Cerebellar hypoplasia
- MedGen UID: 120578
- Concept ID: C0266470
- Finding: Congenital Abnormality
Abnormality of the nervous system
- Corpus callosum, agenesis of
Corpus callosum, agenesis of
- MedGen UID: 104498
- Concept ID: C0175754
- Finding: Congenital Abnormality
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
- Hypoplasia of the corpus callosum
Hypoplasia of the corpus callosum
- MedGen UID: 138005
- Concept ID: C0344482
- Finding: Congenital Abnormality
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
- Intellectual disability, severe
Intellectual disability, severe
- MedGen UID: 48638
- Concept ID: C0036857
- Finding: Mental or Behavioral Dysfunction
Abnormality of the nervous system
- Microlissencephaly
Microlissencephaly
- MedGen UID: 365439
- Concept ID: C1956147
- Finding: Congenital Abnormality
Abnormality of the nervous system
- Poor speech
Poor speech
- MedGen UID: 341172
- Concept ID: C1848207
- Finding: Finding
Abnormality of the nervous system
- Simplified gyral pattern
Simplified gyral pattern
- MedGen UID: 413664
- Concept ID: C2749675
- Finding: Finding
Abnormality of the nervous system
- Small cerebral cortex
Small cerebral cortex
- MedGen UID: 325187
- Concept ID: C1837503
- Finding: Finding
Abnormality of the nervous system
- Arrhinencephaly
- Growth abnormality
- Fetal growth restriction
Fetal growth restriction
- MedGen UID: 4693
- Concept ID: C0015934
- Finding: Pathologic Function
Growth abnormality
- Short stature
Short stature
- MedGen UID: 87607
- Concept ID: C0349588
- Finding: Finding
Growth abnormality
- Fetal growth restriction
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