loading...| Preferred Name |
Axonal neuropathy |
|
| Synonyms |
Axonal neuropathy (disorder) |
|
| ID |
http://purl.bioontology.org/ontology/SNOMEDCT/60703000 |
|
| Active |
1 |
|
| altLabel |
Axonal neuropathy (disorder) |
|
| CASE SIGNIFICANCE ID |
900000000000020002 900000000000448009 |
|
| CTV3ID |
XUHQN |
|
| cui |
C0270921 |
|
| DEFINITION STATUS ID |
900000000000073002 |
|
| Effective time |
20220531 |
|
| Has finding site | ||
| notation |
60703000 |
|
| prefLabel |
Axonal neuropathy |
|
| Subset member |
6011000124106~MAPADVICE~IF OCULAR ANOMALIES, AXONAL NEUROPATHY, DEVELOPMENTAL DELAY SYNDROME CHOOSE F89 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPADVICE~IF CONGENITAL AXONAL NEUROPATHY WITH ENCEPHALOPATHY CHOOSE G93.40 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPADVICE~IF GIANT AXONAL NEUROPATHY CHOOSE G60.8 | 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 6011000124106~MAPTARGET~Q15.9 447562003~MAPRULE~TRUE 6011000124106~MAPADVICE~IF INFANTILE-ONSET AXONAL MOTOR AND SENSORY NEUROPATHY, OPTIC ATROPHY, NEURODEGENERATIVE SYNDROME CHOOSE H47.22 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPTARGET~G93.40 6011000124106~MAPPRIORITY~7 6011000124106~MAPPRIORITY~4 6011000124106~MAPADVICE~IF OCULAR ANOMALIES, AXONAL NEUROPATHY, DEVELOPMENTAL DELAY SYNDROME CHOOSE G60.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPADVICE~MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA 6011000124106~MAPTARGET~P91.819 6011000124106~MAPTARGET~Q87.0 6011000124106~MAPTARGET~ 6011000124106~MAPCATEGORYID~447638001 6011000124106~MAPGROUP~1 6011000124106~MAPGROUP~2 6011000124106~MAPTARGET~G60.8 6011000124106~MAPRULE~IFA 1222704008 | Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy | 6011000124106~MAPADVICE~IF INFANTILE-ONSET AXONAL MOTOR AND SENSORY NEUROPATHY, OPTIC ATROPHY, NEURODEGENERATIVE SYNDROME CHOOSE G60.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPADVICE~IF AXONAL SENSORIMOTOR NEUROPATHY CHOOSE G62.89 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPTARGET~G31.89 447562003~MAPTARGET~G62.8 6011000124106~MAPADVICE~IF INFANTILE-ONSET AXONAL MOTOR AND SENSORY NEUROPATHY, OPTIC ATROPHY, NEURODEGENERATIVE SYNDROME CHOOSE G31.89 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPPRIORITY~8 6011000124106~MAPTARGET~G62.89 6011000124106~MAPADVICE~IF MOEBIUS SYNDROME, AXONAL NEUROPATHY, HYPOGONADOTROPIC HYPOGONADISM SYNDROME CHOOSE G62.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 900000000000508004~ACCEPTABILITYID~900000000000549004 6011000124106~MAPRULE~IFA 230657007 | Axonal sensorimotor neuropathy | 447562003~MAPGROUP~1 6011000124106~MAPRULE~IFA 1237626001 | Congenital axonal neuropathy with encephalopathy | 447562003~CORRELATIONID~447561005 6011000124106~MAPCATEGORYID~447637006 6011000124106~MAPRULE~IFA 711406009 | Autosomal recessive axonal neuropathy with neuromyotonia | 900000000000509007~ACCEPTABILITYID~900000000000548007 6011000124106~MAPTARGET~G71.19 6011000124106~MAPRULE~IFA 724174003 | Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome | 6011000124106~MAPADVICE~IF MOEBIUS SYNDROME, AXONAL NEUROPATHY, HYPOGONADOTROPIC HYPOGONADISM SYNDROME CHOOSE E23.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 900000000000508004~ACCEPTABILITYID~900000000000548007 447562003~MAPADVICE~ALWAYS G62.8 | POSSIBLE REQUIREMENT FOR AN EXTERNAL CAUSE CODE 447562003~MAPPRIORITY~1 447562003~MAPCATEGORYID~447637006 6011000124106~MAPADVICE~IF AUTOSOMAL RECESSIVE LETHAL NEONATAL AXONAL SENSORIMOTOR POLYNEUROPATHY CHOOSE G60.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPRULE~OTHERWISE TRUE 6011000124106~MAPPRIORITY~5 6011000124106~MAPRULE~IFA 230657007 | Axonal sensorimotor neuropathy (disorder) | 6011000124106~MAPRULE~IFA 128207002 | Giant axonal neuropathy (disorder) | 6011000124106~MAPADVICE~ALWAYS G62.9 6011000124106~MAPTARGET~G60.0 6011000124106~MAPPRIORITY~9 6011000124106~MAPCATEGORYID~447639009 6011000124106~MAPADVICE~IF AUTOSOMAL RECESSIVE AXONAL NEUROPATHY WITH NEUROMYOTONIA CHOOSE G71.19 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPRULE~IFA 1172586007 | Ocular anomalies, axonal neuropathy, developmental delay syndrome | 6011000124106~MAPADVICE~IF CONGENITAL AXONAL NEUROPATHY WITH ENCEPHALOPATHY CHOOSE G60.0 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPADVICE~IF OCULAR ANOMALIES, AXONAL NEUROPATHY, DEVELOPMENTAL DELAY SYNDROME CHOOSE Q15.9 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPPRIORITY~1 6011000124106~MAPTARGET~F89 6011000124106~MAPPRIORITY~6 6011000124106~CORRELATIONID~447561005 6011000124106~MAPRULE~IFA 1237626001 | Congenital axonal neuropathy with encephalopathy | AND IFA 445518008 | Age at onset of clinical finding (observable entity) | < 29.0 days 6011000124106~MAPTARGET~G62.9 6011000124106~MAPADVICE~IF AUTOSOMAL RECESSIVE AXONAL NEUROPATHY WITH NEUROMYOTONIA CHOOSE G60.8 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPRULE~IFA 1260129000 | Infantile-onset axonal motor and sensory neuropathy, optic atrophy, neurodegenerative syndrome | 6011000124106~MAPTARGET~E23.0 6011000124106~MAPTARGET~H47.22 6011000124106~MAPADVICE~IF CONGENITAL AXONAL NEUROPATHY WITH ENCEPHALOPATHY AND IF AGE AT ONSET OF CLINICAL FINDING BEFORE 29.0 DAYS CHOOSE P91.819 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPGROUP~3 6011000124106~MAPRULE~IFA 711406009 | Autosomal recessive axonal neuropathy with neuromyotonia (disorder) | 6011000124106~MAPPRIORITY~3 900000000000509007~ACCEPTABILITYID~900000000000549004 900000000000497000~MAPTARGET~XUHQN 6011000124106~MAPPRIORITY~2 6011000124106~MAPRULE~IFA 128207002 | Giant axonal neuropathy | |
|
| tui |
T047 |
|
| Type ID |
900000000000003001 900000000000013009 |
|
| subClassOf |