Cytoscape Web
Click node...


1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
20 signs/symptoms
Lethal arteriopathy syndrome due to FBLN4 deficiency
Acromicric dysplasia

EFEMP2 FBN1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
EFEMP2
(0.76)
FBN1



Citations in the biomedical literature:


Lethal arteriopathy syndrome due to FBLN4 deficiency
EFEMP2
Acromicric dysplasia
FBN1



Lethal arteriopathy syndrome due to FBLN4 deficiency
Acromicric dysplasia

Classification (Orphanet):
- Rare circulatory system disease
- Rare genetic disease
- Rare surgical thoracic disease
Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease

Classification (ICD10):
(no data available)
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: before age 5
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant

External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: C535662

Acromicric dysplasia

Very frequent
- Anomalies of eyelids, eyelashes and lacrimal system
- Anteverted nares / nostrils
- Autosomal dominant inheritance
- Long philtrum
- Round face
- Short hand / brachydactyly
- Short stature / dwarfism / nanism
- Short / small nose
- Small hand / acromicria

Frequent
- Long / large / bulbous nose
- Microstomia / little mouth
- Nerve conduction abnormality
- Thick lips

Occasional
- Abnormal cry / voice / phonation disorder / nasal speech
- Anomalies of spine, vertebrae and pelvis
- Delayed bone age
- Epiphyseal anomaly
- Femur anomaly / absence / agenesis / hypoplasia / bifurcation
- Metacarpal anomalies / Archibald's sign
- Restricted joint mobility / joint stiffness / ankylosis


Lethal arteriopathy syndrome due to FBLN4 deficiency

(no data available)