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1 OMIM reference -
1 associated gene
3 signs/symptoms
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
12 signs/symptoms
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Brachyolmia type 1, Toledo type

APP PAPSS2


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
APP
(0.56)
PAPSS2



Citations in the biomedical literature:


Hereditary cerebral hemorrhage with amyloidosis, Arctic type
APP
Brachyolmia type 1, Toledo type
PAPSS2



Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Brachyolmia type 1, Toledo type

Synonym(s):
- HCHWA, Arctic type

Synonym(s):
(no synonyms)

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

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

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal recessive

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

Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Brachyolmia type 1, Toledo type

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



Very frequent
- Autosomal recessive inheritance
- Corneal clouding / opacity / vascularisation
- Mucopolysacchariduria
- Platyspondyly
- Rib structure anomalies
- Short rib cage / thorax
- Short stature / dwarfism / nanism

Frequent
- Metaphyseal anomaly
- Pelvis anomaly / Narrow / broad iliac wings / pubis abnormality
- Scoliosis
- Short limbs / micromelia / brachymelia

Occasional
- Rachidian / spine canal stenosis