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1 OMIM reference -
1 associated gene
10 signs/symptoms
PROTEIN INTERACTIONS: 1
Metachondromatosis
Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR1 deficiency

PTPN11 IFNGR1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
PTPN11
(0.52)
IFNGR1



Citations in the biomedical literature:


Metachondromatosis
PTPN11
Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR1 deficiency
IFNGR1



Metachondromatosis
Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR1 deficiency

Synonym(s):
(no synonyms)

Synonym(s):
- MSMD due to complete IFNgammaR1 deficiency
- MSMD due to complete interferon gamma receptor 1 deficiency
- Mendelian susceptibility to mycobacterial diseases due to complete interferon gamma receptor 1 deficiency

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

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: normal
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: child / adolescent
Type of inheritance: autosomal recessive

External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
1 MeSH reference: C535530

Metachondromatosis

Very frequent
- Autosomal dominant inheritance
- Bone pain
- Cranial nerves palsy
- Enchondroses
- Epiphyseal anomaly
- Exostoses
- Metaphyseal anomaly
- Osteonecrosis / bone infarction
- Pelvis anomaly / Narrow / broad iliac wings / pubis abnormality
- Periarticular tissue anomaly / extraarticular calcifications



Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR1 deficiency

(no data available)