Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome 1177178005
SNOMED CT code
| SNOMED code | 1177178005 |
|---|---|
| name | Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome |
| status | active |
| date introduced | 2021-10-31 |
| fully specified name(s) | Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome (disorder) |
| synonyms | Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome |
| attributes - group4 | |
| Interprets | Height / growth measure 271603002 |
| attributes - group3 | |
| Finding site | Head structure 69536005 |
| attributes - group2 | |
| Interprets | Head circumference 363812007 |
| Has interpretation | Below reference range 281300000 |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Finding site | Skin structure 39937001 |
| Associated morphology | Hyperpigmentation 4830009 |
| Pathological process | Pathological developmental process 308490002 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Body measurement finding 365605003 Finding of head circumference 301338002 Microcephaly 1148757008 Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome 1177178005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of head 118934005 Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome 1177178005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of pigmentation 414032001 Disorder of skin pigmentation 46690002 Cafe-au-lait spots 201281002 Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome 1177178005 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of general physiological development 271616002 Disorder of stature 237834000 Short stature disorder 237836003 Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome 1177178005 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Inherited cutaneous hyperpigmentation 239079007 Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome 1177178005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome 1177178005 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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