loading...| Preferred Name | Arachnodactyly | |
| Synonyms |
Spider finger Dolichostenomelia Arachnodactyly (disorder) 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 | ||
| Has finding site | ||
| Has pathological process | ||
| notation |
62250003 |
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| Occurs in | ||
| 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 |