Alopecia, epilepsy, intellectual disability syndrome Moynahan type 788417006
SNOMED CT code
| SNOMED code | 788417006 |
|---|---|
| name | Alopecia, epilepsy, intellectual disability syndrome Moynahan type |
| status | active |
| date introduced | 2020-01-31 |
| fully specified name(s) | Alopecia, epilepsy, intellectual disability syndrome Moynahan type (disorder) |
| synonyms |
|
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Finding site | Hair structure 386045008 |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Absence 418560003 |
| attributes - group2 | |
| Finding site | Cerebrum 83678007 |
| Pathological process | Pathological developmental process 308490002 |
| attributes - group3 | |
| Interprets | Intellectual ability 247573007 |
| Has interpretation | Impaired 260379002 |
| attributes - group4 | |
| Interprets | Adaptation behavior 406208005 |
| Has interpretation | Impaired 260379002 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Mental state, behavior and/or psychosocial function finding 384821006 Behavior finding 844005 Intellectual disability 110359009 Alopecia, epilepsy, intellectual disability syndrome Moynahan type 788417006 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Congenital anomaly of integument 38164009 Congenital anomaly of skin 199879009 Congenital anomaly of hair 65033000 Congenital alopecia 2965006 Alopecia, epilepsy, intellectual disability syndrome Moynahan type 788417006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Alopecia, epilepsy, intellectual disability syndrome Moynahan type 788417006 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Alopecia, epilepsy, intellectual disability syndrome Moynahan type 788417006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of nervous system 118940003 Hereditary disorder of nervous system 363235000 Alopecia, epilepsy, intellectual disability syndrome Moynahan type 788417006 SNOMED CT Concept 138875005 Clinical finding 404684003 Central nervous system finding 246556002 Finding of brain 299718000 Seizure 91175000 Seizure disorder 128613002 Epilepsy 84757009 Alopecia, epilepsy, intellectual disability syndrome Moynahan type 788417006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Alopecia, epilepsy, intellectual disability syndrome Moynahan type 788417006 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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