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1 OMIM reference -
1 associated gene
12 signs/symptoms
PROTEIN INTERACTIONS: 1
4 associated genes
No signs/symptoms info
Spondyloenchondrodysplasia
Pediatric systemic lupus erythematosus

ACP5 IRAK1
PTPN22
SPP1
STAT4


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
ACP5
(0.62)
SPP1



Citations in the biomedical literature:


Spondyloenchondrodysplasia
ACP5
Pediatric systemic lupus erythematosus
IRAK1 PTPN22 SPP1 STAT4



Spondyloenchondrodysplasia
Pediatric systemic lupus erythematosus

Synonym(s):
- SPENCD
- Spondyloenchondromatosis
- Spondylometaphyseal dysplasia with enchondromatous changes

Synonym(s):
- SLE, pediatric onset

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

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

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

External references:
1 OMIM reference -
1 MeSH reference: C535782
External references:
No OMIM references
No MeSH references

Spondyloenchondrodysplasia

Very frequent
- Abnormal vertebral size / shape
- Autosomal recessive inheritance
- Enchondroses
- Kyphosis
- Lordosis
- Metaphyseal anomaly
- Rhizomelic micromelia
- Short stature / dwarfism / nanism

Frequent
- Abnormal dentition / dental position / implantation / unerupted / dental ankylosis
- Delayed dentition / eruption of teeth / lack of eruption of teeth
- Epiphyseal anomaly
- Pelvis anomaly / Narrow / broad iliac wings / pubis abnormality



Pediatric systemic lupus erythematosus

(no data available)