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1 OMIM reference -
1 associated gene
21 signs/symptoms
PROTEIN INTERACTIONS: 1
2 OMIM references -
3 associated genes
No signs/symptoms info
Osteoporosis - pseudoglioma
Persistent hyperplastic primary vitreous

LRP5 ATOH7
FZD4
NDP


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
LRP5
(0.63)
NDP



Citations in the biomedical literature:


Osteoporosis - pseudoglioma
LRP5
Persistent hyperplastic primary vitreous
ATOH7 FZD4 NDP



Osteoporosis - pseudoglioma
Persistent hyperplastic primary vitreous

Synonym(s):
- OPPG
- Ocular form of osteogenesis imperfecta

Synonym(s):
- PFVS
- PHPV
- Persistent fetal vasculature syndrome

Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare eye disease
- 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 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
1 MeSH reference: C536063
External references:
2 OMIM references -
1 MeSH reference: D054514

Osteoporosis - pseudoglioma

Very frequent
- Abnormal vertebral size / shape
- Anophthalmos / anophthalmia / microphthalmos / microphthalmia
- Autosomal recessive inheritance
- Bowed diaphysis / diaphyses / long bones
- Cataract / lens opacification
- Delayed bone age
- Hyperextensible joints / articular hyperlaxity
- Hypotonia
- Mutiple fractures / bone fragility
- Osteoporosis / osteopenia / demineralisation / osteomalacia / rickets
- Visual loss / blindness / amblyopia

Frequent
- Intellectual deficit / mental / psychomotor retardation / learning disability
- Pupillary anomalies / mydriasis / myosis / tonic pupil
- Short stature / dwarfism / nanism

Occasional
- Depressed nasal bridge
- Generalized obesity
- Hypotrichosis / atrichia / atrichiasis / scalp hairlessness
- Kyphosis
- Low hair line (back)
- Micrognathia / retrognathia / micrognathism / retrognathism
- Optic nerve anomaly / optic atrophy / anomaly of the papilla


Persistent hyperplastic primary vitreous

(no data available)