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1 OMIM reference -
1 associated gene
12 signs/symptoms
PROTEIN INTERACTIONS: 1
3 OMIM references -
3 associated genes
No signs/symptoms info
Brachyolmia type 1, Toledo type
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia

PAPSS2 HNRNPA1
HNRNPA2B1
VCP


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
PAPSS2
(0.63)
HNRNPA2B1



Citations in the biomedical literature:


Brachyolmia type 1, Toledo type
PAPSS2
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
HNRNPA1 HNRNPA2B1 VCP



Brachyolmia type 1, Toledo type
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia

Synonym(s):
(no synonyms)

Synonym(s):
- IBMPFD
- Limb-girdle muscular dystrophy with Paget disease of bone
- Pagetoid amyotrophic lateral sclerosis
- Pagetoid neuroskeletal syndrome

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

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant

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

Brachyolmia type 1, Toledo type

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


Inclusion body myopathy with Paget disease of bone and frontotemporal dementia

(no data available)