loading...| Preferred Name |
Congenital hypogonadotropic hypogonadism |
|
| Synonyms |
Congenital hypogonadotropic hypogonadism (disorder) |
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| ID |
http://purl.bioontology.org/ontology/SNOMEDCT/722944006 |
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| Active |
1 |
|
| altLabel |
Congenital hypogonadotropic hypogonadism (disorder) |
|
| CASE SIGNIFICANCE ID |
900000000000448009 |
|
| CTV3ID |
XUuuM |
|
| cui |
C3899503 |
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| DEFINITION STATUS ID |
900000000000073002 |
|
| Effective time |
20170131 |
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| Has finding site | ||
| notation |
722944006 |
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| Occurs in | ||
| prefLabel |
Congenital hypogonadotropic hypogonadism |
|
| Subset member |
6011000124106~MAPADVICE~IF CONGENITAL CATARACT WITH INTELLECTUAL DISABILITY AND HYPOGONADOTROPIC HYPOGONADISM SYNDROME CHOOSE E23.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPADVICE~IF MOEBIUS SYNDROME, AXONAL NEUROPATHY, HYPOGONADOTROPIC HYPOGONADISM SYNDROME CHOOSE Q87.0 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 447562003~MAPRULE~TRUE 6011000124106~MAPRULE~IFA 721842008 | Hypogonadotropic hypogonadism with frontoparietal alopecia syndrome (disorder) | 447562003~MAPTARGET~E23.0 6011000124106~MAPTARGET~Q12.0 6011000124106~MAPADVICE~IF HYPOSMIA, NASAL AND OCULAR HYPOPLASIA, HYPOGONADOTROPIC HYPOGONADISM SYNDROME CHOOSE R43.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPPRIORITY~7 6011000124106~MAPPRIORITY~4 6011000124106~MAPRULE~IFA 722027009 | Kallman syndrome with heart disease (disorder) | 6011000124106~MAPADVICE~MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA 6011000124106~MAPTARGET~Q87.0 6011000124106~MAPTARGET~ 6011000124106~MAPCATEGORYID~447638001 6011000124106~MAPADVICE~IF HYPOSMIA, NASAL AND OCULAR HYPOPLASIA, HYPOGONADOTROPIC HYPOGONADISM SYNDROME CHOOSE Q11.2 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPGROUP~1 6011000124106~MAPGROUP~2 6011000124106~MAPRULE~IFA 724281002 | Hyposmia, nasal and ocular hypoplasia, hypogonadotropic hypogonadism syndrome | 6011000124106~MAPPRIORITY~8 447562003~MAPADVICE~ALWAYS E23.0 6011000124106~MAPADVICE~IF MOEBIUS SYNDROME, AXONAL NEUROPATHY, HYPOGONADOTROPIC HYPOGONADISM SYNDROME CHOOSE G62.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPRULE~IFA 721846006 | Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome | 6011000124106~MAPRULE~IFA 721842008 | Hypogonadotropic hypogonadism with frontoparietal alopecia syndrome | 6011000124106~MAPTARGET~K00.0 447562003~MAPGROUP~1 6011000124106~MAPTARGET~F79 447562003~CORRELATIONID~447561005 6011000124106~MAPCATEGORYID~447637006 6011000124106~MAPRULE~IFA 733113002 | Hypogonadotropic hypogonadism retinitis pigmentosa syndrome | 6011000124106~MAPTARGET~G37.9 900000000000509007~ACCEPTABILITYID~900000000000548007 6011000124106~MAPRULE~IFA 724174003 | Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome | 6011000124106~MAPTARGET~H35.52 6011000124106~MAPADVICE~IF MOEBIUS SYNDROME, AXONAL NEUROPATHY, HYPOGONADOTROPIC HYPOGONADISM SYNDROME CHOOSE E23.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPADVICE~ALWAYS E23.0 | DESCENDANTS NOT EXHAUSTIVELY MAPPED 900000000000508004~ACCEPTABILITYID~900000000000548007 6011000124106~MAPADVICE~IF MARTSOLF SYNDROME CHOOSE Q12.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPADVICE~IF CONGENITAL CATARACT WITH INTELLECTUAL DISABILITY AND HYPOGONADOTROPIC HYPOGONADISM SYNDROME CHOOSE F79 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 900000000000497000~MAPTARGET~XUuuM 447562003~MAPPRIORITY~1 6011000124106~MAPADVICE~IF HYPOMYELINATION, HYPOGONADOTROPIC HYPOGONADISM, HYPODONTIA SYNDROME CHOOSE K00.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 447562003~MAPCATEGORYID~447637006 6011000124106~MAPTARGET~I51.9 6011000124106~MAPADVICE~IF HYPOMYELINATION, HYPOGONADOTROPIC HYPOGONADISM, HYPODONTIA SYNDROME CHOOSE E23.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPTARGET~R43.0 6011000124106~MAPADVICE~IF HYPOGONADOTROPIC HYPOGONADISM RETINITIS PIGMENTOSA SYNDROME CHOOSE H35.52 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPADVICE~IF KALLMAN SYNDROME WITH HEART DISEASE CHOOSE I51.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPADVICE~IF MARTSOLF SYNDROME CHOOSE E23.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPADVICE~IF HYPOSMIA, NASAL AND OCULAR HYPOPLASIA, HYPOGONADOTROPIC HYPOGONADISM SYNDROME CHOOSE Q30.1 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPRULE~OTHERWISE TRUE 6011000124106~MAPPRIORITY~5 6011000124106~MAPGROUP~4 6011000124106~MAPRULE~IFA 722380003 | Congenital cataract with intellectual disability and hypogonadotropic hypogonadism syndrome (disorder) | 6011000124106~MAPCATEGORYID~447639009 6011000124106~MAPTARGET~Q30.1 6011000124106~MAPPRIORITY~1 6011000124106~MAPTARGET~L65.9 6011000124106~MAPPRIORITY~6 6011000124106~CORRELATIONID~447561005 6011000124106~MAPADVICE~IF CONGENITAL CATARACT WITH INTELLECTUAL DISABILITY AND HYPOGONADOTROPIC HYPOGONADISM SYNDROME CHOOSE Q12.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPADVICE~IF MARTSOLF SYNDROME CHOOSE F79 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPTARGET~G62.9 6011000124106~MAPTARGET~E23.0 6011000124106~MAPRULE~IFA 721846006 | Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome (disorder) | 6011000124106~MAPRULE~TRUE 6011000124106~MAPTARGET~Q11.2 6011000124106~MAPRULE~IFA 722027009 | Kallman syndrome with heart disease | 6011000124106~MAPRULE~IFA 722380003 | Martsolf syndrome | 6011000124106~MAPADVICE~IF HYPOGONADOTROPIC HYPOGONADISM WITH FRONTOPARIETAL ALOPECIA SYNDROME CHOOSE L65.9 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPGROUP~3 6011000124106~MAPADVICE~IF HYPOSMIA, NASAL AND OCULAR HYPOPLASIA, HYPOGONADOTROPIC HYPOGONADISM SYNDROME CHOOSE E23.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPPRIORITY~3 6011000124106~MAPADVICE~ALWAYS E23.0 6011000124106~MAPADVICE~IF HYPOMYELINATION, HYPOGONADOTROPIC HYPOGONADISM, HYPODONTIA SYNDROME CHOOSE G37.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPPRIORITY~2 |
|
| tui |
T047 |
|
| Type ID |
900000000000003001 900000000000013009 |
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| subClassOf |