SNOMED CT

Last uploaded: January 31, 2024
Preferred Name

Arachnodactyly

Synonyms

Spider finger

Congenital arachnodactyly

ID

http://purl.bioontology.org/ontology/SNOMEDCT/62250003

Active

1

altLabel

Spider finger

Dolichostenomelia

Arachnodactyly (disorder)

Congenital arachnodactyly

CASE SIGNIFICANCE ID

900000000000448009

CTV3ID

Xa86f

cui

C0003706

DEFINITION STATUS ID

900000000000073002

Effective time

20200131

Has associated morphology

http://purl.bioontology.org/ontology/SNOMEDCT/788144009

Has finding site

http://purl.bioontology.org/ontology/SNOMEDCT/82680008

Has pathological process

http://purl.bioontology.org/ontology/SNOMEDCT/308490002

notation

62250003

Occurs in

http://purl.bioontology.org/ontology/SNOMEDCT/255399007

prefLabel

Arachnodactyly

Subset member

6011000124106~MAPADVICE~IF ARACHNODACTYLY WITH ABNORMAL OSSIFICATION AND INTELLECTUAL DISABILITY SYNDROME CHOOSE Q74.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPADVICE~IF CONGENITAL CONTRACTURAL ARACHNODACTYLY CHOOSE Q87.43 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

900000000000497000~MAPTARGET~Xa86f

447562003~MAPRULE~TRUE

6011000124106~MAPADVICE~IF O/E - HANDS - ARACHNODACTYLY CHOOSE Q68.1 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPTARGET~Q87.5

6011000124106~MAPADVICE~IF ARACHNODACTYLY WITH ABNORMAL OSSIFICATION AND INTELLECTUAL DISABILITY SYNDROME CHOOSE Q87.5 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

447562003~MAPTARGET~Q87.4

6011000124106~MAPPRIORITY~4

6011000124106~MAPADVICE~MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA

6011000124106~MAPTARGET~Q87.0

6011000124106~MAPADVICE~IF HARROD SYNDROME CHOOSE Q74.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPTARGET~

6011000124106~MAPCATEGORYID~447638001

6011000124106~MAPADVICE~IF CRANIOFACIAL DIGITAL AND GENITAL ANOMALIES SYNDROME AND IF MALE CHOOSE Q55.9 | MAP IS CONTEXT DEPENDENT FOR GENDER

6011000124106~MAPRULE~IFA 716089008 | Harrod syndrome | AND IFA 248153007 | Male (finding) |

447562003~MAPADVICE~ALWAYS Q87.4

6011000124106~MAPGROUP~1

6011000124106~MAPGROUP~2

6011000124106~MAPRULE~IFA 716089008 | Harrod syndrome |

6011000124106~MAPADVICE~IF HARROD SYNDROME AND IF FEMALE CHOOSE Q52.9 | MAP IS CONTEXT DEPENDENT FOR GENDER

6011000124106~MAPTARGET~Q52.9

6011000124106~MAPRULE~IFA 205821003 | Congenital contractural arachnodactyly (disorder) |

6011000124106~MAPADVICE~IF ARACHNODACTYLY AND INTELLECTUAL DISABILITY WITH FACIAL DYSMORPHISM SYNDROME CHOOSE Q87.0 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPRULE~IFA 720501007 | Arachnodactyly with abnormal ossification and intellectual disability syndrome |

6011000124106~MAPRULE~IFA 720501007 | Arachnodactyly with abnormal ossification and intellectual disability syndrome (disorder) |

900000000000508004~ACCEPTABILITYID~900000000000549004

447562003~MAPGROUP~1

6011000124106~MAPTARGET~F79

447562003~CORRELATIONID~447561005

6011000124106~MAPRULE~IFA 716089008 | Harrod syndrome | AND IFA 248152002 | Female (finding) |

6011000124106~MAPCATEGORYID~447637006

900000000000509007~ACCEPTABILITYID~900000000000548007

6011000124106~MAPADVICE~ALWAYS Q74.8

6011000124106~MAPTARGET~Q74.9

900000000000508004~ACCEPTABILITYID~900000000000548007

6011000124106~MAPTARGET~Q55.9

6011000124106~MAPRULE~IFA 716089008 | Craniofacial digital and genital anomalies syndrome (disorder) |

447562003~MAPPRIORITY~1

447562003~MAPCATEGORYID~447637006

6011000124106~MAPADVICE~IF CRANIOFACIAL DIGITAL AND GENITAL ANOMALIES SYNDROME AND IF FEMALE CHOOSE Q52.9 | MAP IS CONTEXT DEPENDENT FOR GENDER

6011000124106~MAPADVICE~IF ON EXAMINATION - HANDS - ARACHNODACTYLY CHOOSE Q68.1 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPRULE~OTHERWISE TRUE

6011000124106~MAPPRIORITY~5

6011000124106~MAPCATEGORYID~447639009

6011000124106~MAPTARGET~Q87.43

6011000124106~MAPRULE~IFA 164453002 | O/E - hands - arachnodactyly |

6011000124106~MAPADVICE~IF ARACHNODACTYLY AND INTELLECTUAL DISABILITY WITH FACIAL DYSMORPHISM SYNDROME CHOOSE F79 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPADVICE~IF CRANIOFACIAL DIGITAL AND GENITAL ANOMALIES SYNDROME CHOOSE Q74.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPADVICE~IF ARACHNODACTYLY WITH ABNORMAL OSSIFICATION AND INTELLECTUAL DISABILITY SYNDROME CHOOSE F79 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPPRIORITY~1

6011000124106~MAPPRIORITY~6

6011000124106~MAPADVICE~IF HARROD SYNDROME AND IF MALE CHOOSE Q55.9 | MAP IS CONTEXT DEPENDENT FOR GENDER

6011000124106~CORRELATIONID~447561005

6011000124106~MAPTARGET~Q68.1

6011000124106~MAPADVICE~IF HARROD SYNDROME CHOOSE Q87.0 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPTARGET~Q74.8

6011000124106~MAPRULE~IFA 164453002 | On examination - hands - arachnodactyly (disorder) |

6011000124106~MAPGROUP~3

6011000124106~MAPRULE~IFA 205821003 | Congenital contractural arachnodactyly |

6011000124106~MAPPRIORITY~3

6011000124106~MAPADVICE~IF ARACHNODACTYLY AND INTELLECTUAL DISABILITY WITH FACIAL DYSMORPHISM SYNDROME CHOOSE Q74.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

6011000124106~MAPRULE~IFA 720502000 | Arachnodactyly and intellectual disability with facial dysmorphism syndrome |

6011000124106~MAPRULE~IFA 716089008 | Craniofacial digital and genital anomalies syndrome (disorder) | AND IFA 248153007 | Male (finding) |

6011000124106~MAPADVICE~IF CRANIOFACIAL DIGITAL AND GENITAL ANOMALIES SYNDROME CHOOSE Q87.0 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT

900000000000509007~ACCEPTABILITYID~900000000000549004

6011000124106~MAPPRIORITY~2

6011000124106~MAPRULE~IFA 720502000 | Arachnodactyly and intellectual disability with facial dysmorphism syndrome (disorder) |

6011000124106~MAPRULE~IFA 716089008 | Craniofacial digital and genital anomalies syndrome (disorder) | AND IFA 248152002 | Female (finding) |

tui

T019

Type ID

900000000000003001

900000000000013009

subClassOf

http://purl.bioontology.org/ontology/SNOMEDCT/92907008

http://purl.bioontology.org/ontology/SNOMEDCT/445144002

http://purl.bioontology.org/ontology/SNOMEDCT/276655000

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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/MEDDRA/10063847 MEDDRA CUI
http://purl.bioontology.org/ontology/NDFRT/N0000181013 NDFRT CUI
http://purl.bioontology.org/ontology/RCD/XE2uf RCD CUI
http://purl.bioontology.org/ontology/MDRGER/10063847 MDRGER CUI
http://purl.bioontology.org/ontology/SCTSPA/62250003 SCTSPA CUI
http://purl.bioontology.org/ontology/OMIM/MTHU047334 OMIM CUI
http://purl.bioontology.org/ontology/OMIM/MTHU001151 OMIM CUI
http://purl.bioontology.org/ontology/OMIM/MTHU074489 OMIM CUI
http://purl.bioontology.org/ontology/MDRFRE/10063847 MDRFRE CUI
http://purl.bioontology.org/ontology/MESH/D054119 MESH CUI
http://purl.bioontology.org/ontology/CSP/1849-5992 CRISP CUI
http://purl.bioontology.org/ontology/MSHFRE/D054119 MSHFRE CUI
http://purl.bioontology.org/ontology/SNMI/D4-12260 SNMI CUI
http://purl.bioontology.org/ontology/RCD/Xa86f RCD CUI
http://purl.bioontology.org/ontology/OMIM/MTHU012427 OMIM CUI
http://purl.bioontology.org/ontology/OMIM/MTHU016459 OMIM CUI
http://purl.obolibrary.org/obo/HP_0001166 HP LOOM
http://purl.obolibrary.org/obo/HP_0001166 HP LOOM
http://purl.obolibrary.org/obo/MP_0006296 MP LOOM
http://purl.bioontology.org/ontology/RCTV2/PKy7500 RCTV2 LOOM
http://purl.bioontology.org/ontology/MEDDRA/10063847 MEDDRA LOOM
http://www.gamuts.net/entity#arachnodactyly GAMUTS LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C05.660.585.174 RH-MESH LOOM
http://www.owl-ontologies.com/NPOntology.owl#DOID_0050455 NATPRO LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#C0003706 OCHV LOOM
http://www.phoc.org.cn/pmo/class/PMO_00085620 PMAPP-PMO LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU001151 OMIM LOOM
http://www.owl-ontologies.com/OntologyXCT.owl#Arachnodactyly CTX LOOM
http://purl.obolibrary.org/obo/OMIT_0025683 OMIT LOOM
http://purl.obolibrary.org/obo/HP_0001166 UPHENO LOOM
http://purl.org/obo/owl/HP#HP_0001166 BDO LOOM
http://purl.jp/bio/4/id/200906043047524420 IOBC LOOM
http://purl.bioontology.org/ontology/MESH/D054119 MESH LOOM
http://www.semanticweb.org/ontologies/2012/11/abnormalities.owl#phenodb:1549 IFAR LOOM
http://id.nlm.nih.gov/mesh/D054119 MDM LOOM
http://purl.obolibrary.org/obo/MP_0006296 UPHENO LOOM
http://purl.obolibrary.org/obo/MP_0006296 CHIRO LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C16.131.621.585.174 RH-MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#D054119 RH-MESH LOOM
http://purl.bioontology.org/ontology/SNMI/D4-12260 SNMI LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#1411 OCHV LOOM
http://purl.bioontology.org/ontology/RCD/Xa86f RCD LOOM
http://www.gamuts.net/entity#arachnodactyly GAMUTS REST
http://www.gamuts.net/entity#dolichostenomelia GAMUTS REST