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1 OMIM reference -
1 associated gene
24 signs/symptoms
PROTEIN INTERACTIONS: 1
COMMON SIGNS: 10
1 OMIM reference -
1 associated gene
26 signs/symptoms
Pseudoachondroplasia
Spondyloepiphyseal dysplasia congenita

COMP COL2A1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
COMP
(0.52)
COL2A1



Citations in the biomedical literature:


Pseudoachondroplasia
COMP
Spondyloepiphyseal dysplasia congenita
COL2A1



Pseudoachondroplasia
Spondyloepiphyseal dysplasia congenita

Synonym(s):
- Pseudoachondroplastic dysplasia
- Pseudoachondroplastic spondyloepiphyseal dysplasia

Synonym(s):
- Congenital spondyloepiphyseal dysplasia
- SEDC
- Spranger-Wiedemann disease

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

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: neonatal/infancy
Average age of death: normal
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: unknown
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
1 MeSH reference: C535819
External references:
1 OMIM reference -
No MeSH references


COMMON
SIGNS
- Autosomal dominant inheritance
- Epiphyseal anomaly
- Hip dislocation / dysplasia / coxa valga / coxa vara / coxa plana
- Kyphosis
- Lordosis
- Osteoarthritis
- Restricted joint mobility / joint stiffness / ankylosis
- Scoliosis
- Short limbs / micromelia / brachymelia
- Short stature / dwarfism / nanism


Pseudoachondroplasia
Spondyloepiphyseal dysplasia congenita

Very frequent
- Bowed diaphysis / diaphyses / long bones
- Delayed bone age
- Metacarpal anomalies / Archibald's sign
- Metaphyseal anomaly
- Short hand / brachydactyly
- Wrist / carpal anomalies

Frequent
- Abnormal gait
- Articular / joint pain / arthralgia
- Hyperextensible joints / articular hyperlaxity
- Platyspondyly
- Short foot / brachydactyly of toes

Occasional
- Genu valgum
- Genu varum
- Odontoid hypoplasia


Very frequent
- Abnormal vertebral size / shape
- Dysostosis / chondrodysplasia / osteodysplasia / osteochondrosis / skeletal dysplasia
- Narrow rib cage / thorax
- Short neck
- Short rib cage / thorax

Frequent
- Broad forehead
- Cleft palate without cleft lip / submucosal cleft palate / bifid uvula
- Flat face
- Hypertelorism
- Talipes-varus / metatarsal varus

Occasional
- Cataract / lens opacification
- Glaucoma
- Hearing loss / hypoacusia / deafness
- Myopia
- Nystagmus
- Retinal detachment