Severe feeding difficulties, failure to thrive, microcephaly due to ASXL3 deficiency syndrome 773400009
SNOMED CT code
SNOMED code | 773400009 |
---|---|
name | Severe feeding difficulties, failure to thrive, microcephaly due to ASXL3 deficiency syndrome |
status | active |
date introduced | 2019-01-31 |
fully specified name(s) | Severe feeding difficulties, failure to thrive, microcephaly due to ASXL transcriptional regulator 3 deficiency syndrome (disorder) |
synonyms |
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attributes - group1 | |
Associated morphology | Morphologically abnormal structure 49755003 |
Occurrence | Congenital 255399007 |
Pathological process | Pathological developmental process 308490002 |
attributes - group2 | |
Interprets | Intellectual ability 247573007 |
Has interpretation | Impaired 260379002 |
attributes - group3 | |
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 Severe feeding difficulties, failure to thrive, microcephaly due to ASXL3 deficiency syndrome 773400009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 Severe feeding difficulties, failure to thrive, microcephaly due to ASXL3 deficiency syndrome 773400009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Severe feeding difficulties, failure to thrive, microcephaly due to ASXL3 deficiency syndrome 773400009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 Severe feeding difficulties, failure to thrive, microcephaly due to ASXL3 deficiency syndrome 773400009 |
ancestors | sorted most to least specific
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cpt crosswalks |
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