Cytoscape Web
Click node...


1 OMIM reference -
1 associated gene
3 signs/symptoms
PROTEIN INTERACTIONS: 1
2 OMIM references -
4 associated genes
9 signs/symptoms
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Pontocerebellar hypoplasia type 1

APP EXOSC3
RARS2
TSEN54
VRK1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
APP
(0.56)
EXOSC3



Citations in the biomedical literature:


Hereditary cerebral hemorrhage with amyloidosis, Arctic type
APP
Pontocerebellar hypoplasia type 1
EXOSC3 RARS2 TSEN54 VRK1



Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Pontocerebellar hypoplasia type 1

Synonym(s):
- HCHWA, Arctic type

Synonym(s):
- Norman disease
- PCH1

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

Classification (ICD10):
(no data available)
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: before age 5
Type of inheritance: autosomal recessive

External references:
1 OMIM reference -
No MeSH references
External references:
2 OMIM references -
1 MeSH reference: C548069

Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Pontocerebellar hypoplasia type 1

Very frequent
- Autosomal dominant inheritance
- Psychic / behavioural troubles
- Psychic / psychomotor regression / dementia / intellectual decline



Very frequent
- Autosomal recessive inheritance
- Cerebellum / cerebellar vermis anomaly / agenesis / hypoplasia
- Cortical atrophy without hydrocephaly / cerebral hemiatrophy / subcortical atrophy
- Hypertonia / spasticity / rigidity / stiffness
- Microcephaly
- Restricted joint mobility / joint stiffness / ankylosis
- Seizures / epilepsy / absences / spasms / status epilepticus
- Stillbirth / neonatal death

Frequent
- Clinodactyly of fingers 1,2,3,4 / overlapping fingers