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1 OMIM reference -
4 associated genes
8 signs/symptoms
PROTEIN INTERACTIONS: 1
COMMON SIGNS: 4
1 associated gene
24 signs/symptoms
Schizencephaly
Monosomy 9q22.3

COL4A1 PTCH1
EMX2
SHH
SIX3


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
SHH
(0.59)
PTCH1



Citations in the biomedical literature:


Schizencephaly
COL4A1 EMX2 SHH SIX3
Monosomy 9q22.3
PTCH1



Schizencephaly
Monosomy 9q22.3

Synonym(s):
(no synonyms)

Synonym(s):
- Microdeletion 9q22.3

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: no data available
Type of inheritance: sporadic

External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references


COMMON
SIGNS
- Corpus callosum / septum pellucidum total / partial agenesis
- Intellectual deficit / mental / psychomotor retardation / learning disability
- Seizures / epilepsy / absences / spasms / status epilepticus
- Strabismus / squint


Schizencephaly
Monosomy 9q22.3

Very frequent
- EEG anomalies
- Hypertonia / spasticity / rigidity / stiffness
- Porencephaly

Frequent
- Hemiplegia / diplegia / hemiparesia / limb palsy



Very frequent
- Epicanthic folds
- Feeding disorder / dysphagia / swallowing / sucking disorder / esophageal dyskinesia
- Hyperactivity / attention deficit
- Hypotonia
- Low set ears / posteriorly rotated ears
- Macrocephaly / macrocrania / megalocephaly / megacephaly
- Microstomia / little mouth
- Pectus excavatum
- Short neck
- Tall stature / gigantism / growth acceleration
- Trigonocephaly
- Umbilical hernia

Frequent
- Advanced bone age
- Bifid / cleft ear lobe / ear lobe pits
- Delayed dentition / eruption of teeth / lack of eruption of teeth
- Dilated cerebral ventricles without hydrocephaly
- Downslanted palpebral fissures / anti-mongoloid slanting palpebral fissures
- Hyperextensible joints / articular hyperlaxity
- Kyphosis
- Thick / wide ear lobe