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Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
3 OMIM references -
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Familial isolated hypoparathyroidism due to impaired PTH secretion
1 OMIM reference -
2 associated genes
No signs/symptoms info
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Familial isolated hypoparathyroidism due to impaired PTH secretion

HNRNPA1
(UniProt - OMIM)
 CASR
(UniProt - OMIM)
HNRNPA2B1
(UniProt - OMIM)
 PTH
(UniProt - OMIM)
VCP
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
VCP
(0.63)
CASR


Citations in the biomedical literature:


Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
HNRNPA1 HNRNPA2B1 VCP
Familial isolated hypoparathyroidism due to impaired PTH secretion
CASR PTH



Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Familial isolated hypoparathyroidism due to impaired PTH secretion

Synonym(s):
- IBMPFD
- Limb-girdle muscular dystrophy with Paget disease of bone
- Pagetoid amyotrophic lateral sclerosis
- Pagetoid neuroskeletal syndrome
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
External references:
3 OMIM references -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.