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6 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
25 signs/symptoms
Fetal and neonatal alloimmune thrombocytopenia
Spondyloepimetaphyseal dysplasia congenita, Strudwick type

CD109 COL2A1
GP1BA
GP1BB
ITGA2
ITGA2B
ITGB3


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
ITGA2B
(0.85)
COL2A1



Citations in the biomedical literature:


Fetal and neonatal alloimmune thrombocytopenia
CD109 GP1BA GP1BB ITGA2 ITGA2B ITGB3

Spondyloepimetaphyseal dysplasia congenita, Strudwick type
COL2A1



Fetal and neonatal alloimmune thrombocytopenia
Spondyloepimetaphyseal dysplasia congenita, Strudwick type

Synonym(s):
- NAIT

Synonym(s):
(no synonyms)

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

Classification (ICD10):
- Certain conditions originating in the perinatal period -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

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

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

Spondyloepimetaphyseal dysplasia congenita, Strudwick type

Very frequent
- Autosomal dominant inheritance
- Dysostosis / chondrodysplasia / osteodysplasia / osteochondrosis / skeletal dysplasia
- Epiphyseal anomaly
- Lordosis
- Metaphyseal anomaly
- Platyspondyly
- Short limbs / micromelia / brachymelia
- Short rib cage / thorax
- Short stature / dwarfism / nanism

Frequent
- Abnormal gait
- Cleft palate without cleft lip / submucosal cleft palate / bifid uvula
- Femur anomaly / absence / agenesis / hypoplasia / bifurcation
- Flat face
- Genu valgum
- Hip dislocation / dysplasia / coxa valga / coxa vara / coxa plana
- Hypertelorism
- Kyphosis
- Myopia
- Osteoarthritis
- Retinal detachment

Occasional
- Genu varum
- Odontoid hypoplasia
- Respiratory distress / dyspnea / respiratory failure / lung volume reduction
- Scoliosis
- Talipes-varus / metatarsal varus


Fetal and neonatal alloimmune thrombocytopenia

(no data available)