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Polydactyly (CUI C0152427) Suggest changes to this concept
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Terms & Properties

Concept Unique Identifier (CUI): C0152427

NCI Thesaurus Code: C87110  (see NCI Thesaurus info)

Semantic Type: Congenital Abnormality

NCIt Definition: A congenital abnormality characterized by more than 5 digits on a hand or foot.

GARD Definition: Polydactyly is a condition in which a person has more than five fingers per hand or five toes per foot. It is the most common birth defect of the hand and foot. Polydactyly can occur as an isolated finding such that the person has no other physical anomalies or intellectual impairment. However, it can occur in association with other birth defects and cognitive abnormalities as part of a genetic syndrome. In some cases, the extra digits may be well-formed and functional. Surgery may be considered especially for poorly formed digits or very large extra digits. Surgical management depends greatly on the complexity of the deformity.
- this information is from GARD/ORDR/NCATS.

HPO Definition: A congenital anomaly characterized by the presence of supernumerary fingers or toes. [HPO:probinson]

MSH Definition: A congenital anomaly of the hand or foot, marked by the presence of supernumerary digits.

Synonyms & Abbreviations: (see Synonym Details)
Accessory digit
Extra digits
Hyperdactylies
Hyperdactyly
Multiple digits
Polydactylias
Polydactylia
Polydactylies
Polydactylisms
Polydactylism
Polydactyly (disorder)
Polydactyly [Disease/Finding]
Polydactyly NOS
Polydactyly, unspecified digits
Polydactyly, unspecified
polydactyly
Supernumerary digit(s) NOS
Supernumerary digits
Supernumerary digit

External Source Codes: 
NCI Thesaurus Code C87110 (see NCI Thesaurus info)

Other Properties: Property Definitions
Name Value Source
ACTIVE 1 SNOMEDCT_US
AN do not confuse with SYNDACTYLY; coord IM with FINGERS /abnorm (IM) or TOES /abnorm (IM); SHORT RIB-POLYDACTYLY SYNDROME is also available MSH
AQL BL CF CI CL CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI MSH
CASE_SIGNIFICANCE_ID 900000000000448009 SNOMEDCT_US
CHARACTERISTIC_TYPE_ID 900000000000011006 SNOMEDCT_US
Contributing_Source NICHD NCI
CTV3ID PF0.. SNOMEDCT_US
DATE_CREATED 2009-07-29T01:39:27Z HPO
DATE_CREATED 2013-01-09T00:04:00 GARD
DATE_LAST_MODIFIED 2013-01-09T00:04:00 GARD
DC 1 MSH
DEFINITION_STATUS_ID 900000000000073002 SNOMEDCT_US
DISEASE_IDENTIFIER_ID 14138 GARD
DISEASE_IDENTIFIER_ID 14139 GARD
DISEASE_IDENTIFIER_ID 14140 GARD
DISEASE_IDENTIFIER_ID 14141 GARD
DISEASE_IDENTIFIER_ID 14142 GARD
DX 19940101 MSH
EFFECTIVE_TIME 20070731 SNOMEDCT_US
FX D013576 MSH
HAS_GARD_PAGE true GARD
HN 94 MSH
IAN DEFAULT ICD10
ICE Supernumerary digits ICD9CM
IDENTIFIER_TYPE_ID 1 GARD
INCLUSION_TERM Supernumerary digit(s) NOS ICD10
IS_ACTIVE true GARD
IS_RARE true GARD
IS_SPANISH false GARD
MDA 19921228 MSH
MESH_DEFINITION A congenital anomaly of the hand or foot, marked by the presence of supernumerary digits. NDFRT
MESH_DUI D017689 NDFRT
MESH_NAME Polydactyly NDFRT
MESH_UI M0026754 NDFRT
MIMTYPE 3 OMIM
MIMTYPEMEANING Phenotype description, molecular basis known. OMIM
MIMTYPEVALUE pound OMIM
MMR 20120703 MSH
MN C05.660.585.600 MSH
MN C16.131.621.585.600 MSH
MODIFIER_ID 900000000000451002 SNOMEDCT_US
NDFRT_KIND DISEASE_KIND NDFRT
NICHD_Hierarchy_Term Polydactyly NCI
NUI N0000003623 NDFRT
ORDER_NO 27848 ICD10CM
ORDER_NO 27852 ICD10CM
PM 94 MSH
PRIMARY_PATH 10036063$10028381$10028396$10010331$Polydactyly$Musculoskeletal and connective tissue disorders of limbs congenital$Musculoskeletal and connective tissue disorders congenital$Congenital, familial and genetic disorders MDR
PRIMARY_SOC 10010331 MDR
PT_IN_VERSION 10.0 MDR
PT_IN_VERSION 10.1 MDR
PT_IN_VERSION 11.0 MDR
PT_IN_VERSION 11.1 MDR
PT_IN_VERSION 12.0 MDR
PT_IN_VERSION 12.1 MDR
PT_IN_VERSION 13.0 MDR
PT_IN_VERSION 13.1 MDR
PT_IN_VERSION 14.0 MDR
PT_IN_VERSION 14.1 MDR
PT_IN_VERSION 15.0 MDR
PT_IN_VERSION 15.1 MDR
PT_IN_VERSION 16.0 MDR
PT_IN_VERSION 16.1 MDR
PT_IN_VERSION 17.0 MDR
PT_IN_VERSION 17.1 MDR
PT_IN_VERSION 18.0 MDR
PT_IN_VERSION 18.1 MDR
PT_IN_VERSION 19.0 MDR
PT_IN_VERSION 19.1 MDR
PT_IN_VERSION 20.0 MDR
PT_IN_VERSION 20.1 MDR
PT_IN_VERSION 8.0 MDR
PT_IN_VERSION 8.1 MDR
PT_IN_VERSION 9.0 MDR
PT_IN_VERSION 9.1 MDR
RARE_DISEASE_URL http://rarediseases.info.nih.gov/gard/4410/polydactyly/resources/1 GARD
RXAUI 3174238 RXNORM
RXAUI 3222048 RXNORM
RXAUI 3222051 RXNORM
RXAUI 3222053 RXNORM
RXAUI 3222054 RXNORM
RXCUI 1022588 RXNORM
SID HP:0006034 HPO
SID HP:0006046 HPO
SID HP:0006123 HPO
SID HP:0009605 HPO
SMQ_TERM_ADDVERSION 10.0 MDR
SMQ_TERM_CAT A MDR
SMQ_TERM_LEVEL 4 MDR
SMQ_TERM_LEVEL 5 MDR
SMQ_TERM_LMVERSION 14.0 MDR
SMQ_TERM_SCOPE 2 MDR
SMQ_TERM_STATUS A MDR
SMQ_TERM_WEIGHT 0 MDR
SNOMED_CID 205120004 NDFRT
SNOMED_CID 367506006 NDFRT
SUBSET_MEMBER 447562003~CORRELATIONID~447561005 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPADVICE~ALWAYS Q69.9 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPCATEGORYID~447637006 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPGROUP~1 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPPRIORITY~1 SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPRULE~TRUE SNOMEDCT_US
SUBSET_MEMBER 447562003~MAPTARGET~Q69.9 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~CORRELATIONID~447561005 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPADVICE~ALWAYS Q69.9 | DESCENDANTS NOT EXHAUSTIVELY MAPPED SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPCATEGORYID~447637006 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPGROUP~1 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPPRIORITY~1 SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPRULE~TRUE SNOMEDCT_US
SUBSET_MEMBER 6011000124106~MAPTARGET~Q69.9 SNOMEDCT_US
SUBSET_MEMBER 900000000000497000~MAPTARGET~PF0.. SNOMEDCT_US
SUBSET_MEMBER 900000000000508004~ACCEPTABILITYID~900000000000548007 SNOMEDCT_US
SUBSET_MEMBER 900000000000508004~ACCEPTABILITYID~900000000000549004 SNOMEDCT_US
SUBSET_MEMBER 900000000000509007~ACCEPTABILITYID~900000000000548007 SNOMEDCT_US
SUBSET_MEMBER 900000000000509007~ACCEPTABILITYID~900000000000549004 SNOMEDCT_US
TERMUI T052912 MSH
TERMUI T052913 MSH
TERMUI T052914 MSH
TERMUI T052915 MSH
TH NLM (1994) MSH
TH OMIM (2013) MSH
TYPE_ID 900000000000003001 SNOMEDCT_US
TYPE_ID 900000000000013009 SNOMEDCT_US

Additional Concept Data:  (none)

URL to Bookmark: https://ncim-stage.nci.nih.gov/ncimbrowser/ConceptReport.jsp?dictionary=NCI Metathesaurus&code=C0152427

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