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1 OMIM reference -
1 associated gene
11 signs/symptoms
PROTEIN INTERACTIONS: 1
6 OMIM references -
7 associated genes
No signs/symptoms info
Hypoplasminogenemia
Immunodeficiency due to a late component of complements deficiency

PLG C5
C6
C7
C8A
C8B
C8G
C9


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
PLG
(0.75)
C7



Citations in the biomedical literature:


Hypoplasminogenemia
PLG
Immunodeficiency due to a late component of complements deficiency
C5 C6 C7 C8A C8B C8G
C9



Hypoplasminogenemia
Immunodeficiency due to a late component of complements deficiency

Synonym(s):
- Plasminogen deficiency type 1

Synonym(s):
- Deficiency of complement of terminal pathway
- Immunodeficiency due to a C5 to C9 component complement deficiency

Classification (Orphanet):
- Rare genetic disease
- Rare systemic or rheumatologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease

Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
(no data available)

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

Hypoplasminogenemia

Very frequent
- Anomalies of eyes and vision

Frequent
- Anomalies of tongue, gingiva and oral mucosa

Occasional
- Abnormal / polycystic ovaries
- Anomalies of skin, subcutaneous tissue and mucosae
- Dandy-Walker anomaly
- Hydrocephaly
- Intestinal / colonic anomaly
- Structural anomalies of middle ear / ossicles / tympanic cavity
- Structural anomalies of the respiratory system and diaphragm
- Urinary / renal lithiasis / kidney stones / nephritic colic
- Uterine / uterus / Fallopian tubes anomalies


Immunodeficiency due to a late component of complements deficiency

(no data available)