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Retinopathy of prematurity
1 OMIM reference -
3 associated genes
25 connected diseases
No signs/symptoms info
Disease Type of connection
Familial exudative vitreoretinopathy
Persistent hyperplastic primary vitreous
Idiopathic juvenile osteoporosis
Coats disease
Norrie disease
Hyperostosis corticalis generalisata
Autosomal dominant osteopetrosis type 1
Autosomal dominant osteosclerosis, Worth type
Osteoporosis - pseudoglioma
Osteosclerosis - developmental delay - craniosynostosis
Craniodiaphyseal dysplasia
Sclerosteosis
Dominant hypophosphatemia with nephrolithiasis or osteoporosis
Familial isolated dilated cardiomyopathy
Heritable pulmonary arterial hypertension
Muscular dystrophy, Selcen type
Early-onset autosomal dominant Alzheimer disease
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Hereditary cerebral hemorrhage with amyloidosis, Dutch type
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Hereditary cerebral hemorrhage with amyloidosis, Iowa type
Hereditary cerebral hemorrhage with amyloidosis, Italian type
Hereditary cerebral hemorrhage with amyloidosis, Piedmont type
Osteogenesis imperfecta type 3
Osteogenesis imperfecta type 4
Synonym(s):
- ROP
- Retrolental fibroplasia
Classification (Orphanet):
- Rare eye disease
Classification (ICD10):
- Diseases of the eye and adnexa -
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
1 MeSH reference: D012178
Gene symbol UniProt reference OMIM reference
FZD4 Q9ULV1604579
LRP5 O75197603506
NDP Q00604300658
No signs/symptoms info available.