Norrie disease https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/5588 https://github.com/monarch-initiative/mondo/issues/8986 https://rarediseases.info.nih.gov/diseases/7224/norrie-disease https://www.malacards.org/card/norrie_disease Episkopi blindness pseudoglioma Anderson-Warburg syndrome atrophia bulborum hereditaria Norrie-Warburg disease foetal iritis syndrome ND Norrie disease MEDGEN:75615 GARD:0007224 NCIT:C118634 SCTID:15228007 Norrie-Warburg syndrome DOID:0060844 ICD9:743.8 A rare X-linked genetic vitreoretinal condition characterized by abnormal retinal development with congenital blindness. Common associated manifestations include sensorineural hearing loss and developmental delay, intellectual disability and/or behavioral disorders. Norrie disease, X-linked recessive Norrie syndrome MedDRA:10069760 NORD:1514 fetal iritis syndrome OMIM:310600 NDP MESH:C537849 icd11.foundation:676214590 MONDO:0010691 UMLS:C0266526 Orphanet:649 X-linked syndromic intellectual disability congenital vitreoretinal dysplasia NDP-related vitreoretinopathy