coloboma of iris

congenital or acquired defect characterized by the presence of a hole in or adjacent to the iris
rdfs:label
"coloboma of iris"@en
skos:altLabel
"Coloboma of iris"@en
"Coloboma of the Iris"@en
schema:description "congenital or acquired defect characterized by the presence of a hole in or adjacent to the iris"@en
schema:dateModified "2026-10-24T00:52:06+00:00"^^xsd:dateTime
schema:version 2560169589
wikibase:identifiers 11
9
wikibase:sitelinks 0
wikibase:statements 21
p:P14914 wd:statement/Q56014419-C77A4A6B-4340-490E-B80D-860AAB0E1932
p:P1550 wd:statement/Q56014419-BA8D9B4F-AFB8-48EE-92DA-C330BE33001C
p:P1748 wd:statement/Q56014419-80DACA95-A98A-4B89-864B-AF702E529C4D
p:P2293 wd:statement/Q56014419-797EFBBC-6BDA-4AE7-A3EF-1B528930ECED
wd:statement/Q56014419-86C982D6-24D1-420A-B3A0-0B3727429079
wd:statement/Q56014419-ACFEDCEB-1A45-4749-9CEC-565EECFA5250
wd:statement/Q56014419-CA377A95-5278-44D7-BA36-13DC60761D45
wd:statement/Q56014419-DC417ECF-DD5A-464F-8FC4-67C920EBE5EF
p:P279 wd:statement/Q56014419-6250ef50-44f1-b303-4197-34b90799afdc
wd:statement/Q56014419-f1b179e8-498a-ab4d-01e4-2c06d6853b2d
p:P2888 wd:statement/Q56014419-06A51B67-63EF-4D4E-9143-8DC1B1AAB8BA
wd:statement/Q56014419-4B01F9B9-A348-4F08-B394-AEA2171C5664
p:P2892 wd:statement/Q56014419-08FAA10C-603D-4D61-ACED-C167FED3FFAD
wd:statement/Q56014419-40FE19FA-CEC0-4996-A653-FF5F55444AE8
p:P31 wd:statement/Q56014419-0127B2C9-F543-4FC4-9D00-70E004C7E8BC
p:P3841 wd:statement/Q56014419-0CD00749-1649-4D7C-B7B6-D40DCA30E0B1
p:P4229 wd:statement/Q56014419-7711C15B-F181-4883-B502-346590121BA3
p:P4317 wd:statement/Q56014419-B3FFB9B4-5264-423C-B0FE-AF0B407529DC
p:P5270 wd:statement/Q56014419-6F4DBFF4-048D-4C27-9120-840F4AA322F8
p:P7329 wd:statement/Q56014419-E5820357-1C61-4175-AD4D-311173C6AB23
p:P7807 wd:statement/Q56014419-511626C1-B4BA-4893-88F9-C429C052C7FC
p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0020356>
wdt:P14914 "D98944"
wdt:P1550 "98944"
wdt:P1748 "C98879"
wdt:P2293 PAX6
ACTG1
SALL2
FZD5
ABCB6
wdt:P279 coloboma
iris disease
wdt:P2888 <http://purl.obolibrary.org/obo/HP_0000612>
<http://www.orpha.net/ORDO/Orphanet_98944>
wdt:P2892 "C0240063"
"C0266551"
wdt:P31 type of disease
wdt:P3841 "HP:0000612"
wdt:P4229 "Q13.0"
wdt:P4317 "1434"
wdt:P5270 "MONDO_0020356"
wdt:P7329 "LA11.4"
wdt:P7807 "1552972259"
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