loading...| Preferred Name | Congenital anomaly of endocrine gonad | |
| Synonyms |
Congenital anomaly of endocrine gonad (disorder) |
|
| ID |
http://purl.bioontology.org/ontology/SNOMEDCT/371118004 |
|
| Active |
1 |
|
| altLabel |
Congenital anomaly of endocrine gonad (disorder) |
|
| CASE SIGNIFICANCE ID |
900000000000448009 |
|
| CTV3ID |
XUUiV |
|
| cui |
C1299566 |
|
| DEFINITION STATUS ID |
900000000000073002 |
|
| Effective time |
20020731 |
|
| Has associated morphology | ||
| Has finding site | ||
| Has pathological process | ||
| notation |
371118004 |
|
| Occurs in | ||
| prefLabel |
Congenital anomaly of endocrine gonad |
|
| Subset member |
6011000124106~MAPTARGET~Q55.20 6011000124106~MAPRULE~IFA 725029001 | Frontonasal dysplasia with alopecia and genital anomaly syndrome | AND IFA 248153007 | Male (finding) | 6011000124106~MAPADVICE~IF LUNG FIBROSIS, IMMUNODEFICIENCY, 46,XX GONADAL DYSGENESIS SYNDROME CHOOSE Q99.1 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPRULE~IFA 725029001 | Frontonasal dysplasia with alopecia and genital anomaly syndrome | AND IFA 248152002 | Female (finding) | 447562003~MAPRULE~TRUE 447562003~MAPTARGET~Q89.2 6011000124106~MAPADVICE~IF LUNG FIBROSIS, IMMUNODEFICIENCY, 46,XX GONADAL DYSGENESIS SYNDROME CHOOSE D84.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPRULE~IFA 56212008 | Leydig cell agenesis | 6011000124106~MAPPRIORITY~7 6011000124106~MAPPRIORITY~4 6011000124106~MAPTARGET~Q30.8 6011000124106~MAPTARGET~J84.10 6011000124106~MAPADVICE~MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA 6011000124106~MAPADVICE~IF FRONTONASAL DYSPLASIA WITH ALOPECIA AND GENITAL ANOMALY SYNDROME AND IF FEMALE CHOOSE Q52.9 | MAP IS CONTEXT DEPENDENT FOR GENDER 6011000124106~MAPTARGET~D84.9 6011000124106~MAPTARGET~ 6011000124106~MAPCATEGORYID~447638001 6011000124106~MAPRULE~IFA 371122009 | Congenital anomaly of endocrine testis | 6011000124106~MAPGROUP~1 6011000124106~MAPGROUP~2 6011000124106~MAPRULE~IFA 721977007 | Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome | 6011000124106~MAPRULE~IFA 370966000 | Congenital anomaly of endocrine ovary (disorder) | 6011000124106~MAPPRIORITY~10 6011000124106~MAPTARGET~Q52.9 6011000124106~MAPTARGET~Q96.9 6011000124106~MAPADVICE~IF LEYDIG CELL AGENESIS CHOOSE Q55.29 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPPRIORITY~8 6011000124106~MAPADVICE~IF 46,XY PARTIAL GONADAL DYSGENESIS CHOOSE Q56.1 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPRULE~IFA 205683001 | Ovarian dysgenesis | 447562003~MAPGROUP~1 447562003~CORRELATIONID~447561005 6011000124106~MAPCATEGORYID~447637006 900000000000509007~ACCEPTABILITYID~900000000000548007 6011000124106~MAPRULE~IFA 83579008 | Mixed gonadal dysgenesis (disorder) | 6011000124106~MAPRULE~IFA 205683001 | Ovarian dysgenesis (disorder) | 6011000124106~MAPADVICE~IF CONGENITAL ANOMALY OF ENDOCRINE OVARY CHOOSE Q50.39 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPADVICE~IF OVARIAN DYSGENESIS CHOOSE Q96.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 900000000000497000~MAPTARGET~XUUiV 6011000124106~MAPADVICE~IF FRONTONASAL DYSPLASIA WITH ALOPECIA AND GENITAL ANOMALY SYNDROME CHOOSE Q30.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPTARGET~Q50.39 900000000000508004~ACCEPTABILITYID~900000000000548007 6011000124106~MAPADVICE~IF FRONTONASAL DYSPLASIA WITH ALOPECIA AND GENITAL ANOMALY SYNDROME CHOOSE Q84.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPTARGET~Q55.9 6011000124106~MAPADVICE~IF MIXED GONADAL DYSGENESIS CHOOSE Q96.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPRULE~IFA 371122009 | Congenital anomaly of endocrine testis (disorder) | 447562003~MAPPRIORITY~1 6011000124106~MAPADVICE~IF CONGENITAL ANOMALY OF ENDOCRINE TESTIS CHOOSE Q55.20 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 447562003~MAPCATEGORYID~447637006 6011000124106~MAPRULE~IFA 95198001 | Pure gonadal dysgenesis 46,XX | 6011000124106~MAPRULE~IFA 95198001 | Pure gonadal dysgenesis 46,XX (disorder) | 6011000124106~MAPRULE~OTHERWISE TRUE 6011000124106~MAPTARGET~Q96.8 6011000124106~MAPPRIORITY~5 6011000124106~MAPRULE~IFA 725045004 | 46,XY partial gonadal dysgenesis | 6011000124106~MAPADVICE~IF PURE GONADAL DYSGENESIS 46,XX CHOOSE Q99.1 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPPRIORITY~9 6011000124106~MAPCATEGORYID~447639009 6011000124106~MAPRULE~IFA 721977007 | Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome (disorder) | 6011000124106~MAPADVICE~ALWAYS Q89.2 | DESCENDANTS NOT EXHAUSTIVELY MAPPED 6011000124106~MAPADVICE~IF LUNG FIBROSIS, IMMUNODEFICIENCY, 46,XX GONADAL DYSGENESIS SYNDROME CHOOSE J84.10 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPADVICE~IF LUNG FIBROSIS, IMMUNODEFICIENCY, 46,XX GONADAL DYSGENESIS SYNDROME CHOOSE Q99.1 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPTARGET~Q56.1 6011000124106~MAPPRIORITY~1 6011000124106~MAPTARGET~Q55.29 6011000124106~MAPADVICE~ALWAYS Q89.2 6011000124106~MAPPRIORITY~6 6011000124106~MAPRULE~IFA 83579008 | Mixed gonadal dysgenesis | 6011000124106~CORRELATIONID~447561005 6011000124106~MAPRULE~TRUE 6011000124106~MAPTARGET~Q84.0 6011000124106~MAPGROUP~3 6011000124106~MAPRULE~IFA 725029001 | Frontonasal dysplasia with alopecia and genital anomaly syndrome | 447562003~MAPADVICE~ALWAYS Q89.2 6011000124106~MAPPRIORITY~3 6011000124106~MAPTARGET~Q89.2 6011000124106~MAPTARGET~Q99.1 6011000124106~MAPADVICE~IF FRONTONASAL DYSPLASIA WITH ALOPECIA AND GENITAL ANOMALY SYNDROME AND IF MALE CHOOSE Q55.9 | MAP IS CONTEXT DEPENDENT FOR GENDER 6011000124106~MAPPRIORITY~2 6011000124106~MAPRULE~IFA 56212008 | Leydig cell agenesis (disorder) | 6011000124106~MAPRULE~IFA 370966000 | Congenital anomaly of endocrine ovary | |
|
| tui |
T019 |
|
| Type ID |
900000000000003001 900000000000013009 |
|
| subClassOf |
http://purl.bioontology.org/ontology/SNOMEDCT/205681004 |
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://purl.bioontology.org/ontology/SCTSPA/371118004 | SCTSPA | CUI |