deformity of chest and rib

human disease
rdfs:label
"deformity of chest and rib"@en
skos:altLabel "Malformation thoracique"@fr
schema:description
"human disease"@en
schema:dateModified "2026-10-23T23:33:14+00:00"^^xsd:dateTime
schema:version 2560155957
wikibase:identifiers 8
wikibase:sitelinks 1
wikibase:statements 53
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wd:statement/Q25377767-4D69D3E0-89E8-4E2F-BABE-74DE8BCD4314
p:P2888 wd:statement/Q25377767-E2748D9B-F1E2-4E91-804B-A525B651432A
p:P2892 wd:statement/Q25377767-C024670A-C496-4CF6-95E3-D050E4D6FCB4
p:P31 wd:statement/Q25377767-C0292633-0953-4AFD-A69B-8163AC45E24E
p:P3201 wd:statement/Q25377767-E4AAE328-50E8-4C2B-B9DD-66A897D09435
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p:direct-normalized/P3201 <http://purl.bioontology.org/ontology/MDRFRE/10061810>
p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0015929>
wdt:P14914 "D182108"
wdt:P1550 "182108"
wdt:P2293 MYOD1
GLI1
EVC
GLE1
MUSK
NEK1
NUP88
PRKACB
RAPSN
SLC18A3
WNT7B
TUBA1A
IFT140
KIAA0586
KIAA0753
TCTN3
TRAF3IP1
IFT172
INTU
IFT81
IFT52
DYNC2LI1
MAGEL2
DYNC2I1
KIF21A
IFT122
WDR35
IFT80
WDR19
DYNC2H1
TTC21B
CSPP1
DYNC2I2
NEK9
IFT43
EVC2
CEP120
DYNLT2B
DOK7
GLDN
Receptor for retinol uptake STRA6
wdt:P279 deformity
respiratory or thoracic malformation
wdt:P2888 <http://www.orpha.net/ORDO/Orphanet_182108>
wdt:P2892 "C5680597"
wdt:P31 type of disease
wdt:P3201 "10061810"
wdt:P494 "M95.4"
wdt:P5270 "MONDO_0015929"
wdt:P7329 "FC00.2"
wdt:P7807 "717631649"
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