Nance-Horan syndrome

disorder of lens
rdfs:label
"Nance-Horan syndrome"@en
skos:altLabel "Cataract X-linked with Hutchinsonian teeth"@en
"Cataract dental syndrome"@en
"Cataract, X-Linked, With Hutchinsonian Teeth"@en
"Cataract-Dental Syndrome"@en
"Mesiodens cataract syndrome"@en
"Mesiodens-Cataract Syndrome"@en
"NANCE-HORAN SYNDROME"@en
"NANCE-HORAN SYNDROME; NHS"@en
"NHS"@en
"Nance–Horan syndrome"@en
schema:description
"disorder of lens"@en
schema:dateModified "2026-10-24T00:28:25+00:00"^^xsd:dateTime
schema:version 2560166103
wikibase:identifiers 13
wikibase:sitelinks 5
wikibase:statements 47
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p:P2581 wd:statement/Q17144153-23017A53-B729-41E8-80EF-8197A0A7CD58
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p:P31 wd:statement/Q17144153-48F258EF-A551-4540-AC84-A0463C4A1450
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p:P665 wd:statement/Q17144153-165AA394-75F9-470F-B98D-7060DF37714C
p:P699 wd:statement/Q17144153-2D193879-4ED1-451A-81C3-F33A151CE67A
p:direct-normalized/P2581 <http://babelnet.org/rdf/s16633600n>
p:direct-normalized/P486 <http://id.nlm.nih.gov/mesh/C538336>
p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0010545>
p:direct-normalized/P6366 <https://makg.org/entity/2780437957>
p:direct-normalized/P665 <http://www.kegg.jp/entry/H01292>
p:direct-normalized/P699 <http://purl.obolibrary.org/obo/DOID_DOID:0060599>
wdt:P11430 "DI-02027"
wdt:P14914 "D00627"
wdt:P1550 "627"
wdt:P1692 "759.89"
wdt:P1995 medical genetics
wdt:P2293 NHS
wdt:P2581 "16633600n"
wdt:P279 syndrome
X-linked dominant disease
multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome
malformation syndrome with odontal and/or periodontal component
rare genetic developmental defect during embryogenesis
dentocutaneous disease with cataract
X-linked intellectual disability
wdt:P2841 neonatal onset
wdt:P2888 <http://identifiers.org/doid/DOID:0060599>
<http://purl.obolibrary.org/obo/DOID_0060599>
<http://www.orpha.net/ORDO/Orphanet_627>
wdt:P2892 "C0796085"
wdt:P31 type of disease
rare disease
wdt:P4229 "Q87.0"
wdt:P4317 "7161"
wdt:P486 "C538336"
wdt:P492 "302350"
wdt:P5008 WikiProject Medicine
wdt:P5270 "MONDO_0010545"
wdt:P6366 "2780437957"
wdt:P6532 acute visual loss
cataract
microphthalmia
glaucoma
strabismus
pathologic nystagmus
narrow face
behavioral abnormality
disability affecting intellectual abilities
prominent ear
progenism
hyperdontia
tooth abnormality
retinal detachment
visual impairment
wdt:P665 "H01292"
wdt:P699 "DOID:0060599"
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