Family history of congenital disease 160417009

SNOMED CT code

SNOMED code

160417009

name

Family history of congenital disease

status

active

date introduced

2002-01-31

fully specified name(s)

Family history of congenital disease (situation)

synonyms

Family history of congenital anomaly
Family history of congenital disease

attributes - group1

Finding context

Known present 410515003

Associated finding

Congenital disease 66091009

Subject relationship context

Person in the family 303071001

Temporal context

Current or past 410511007

parents

Family history of disorder 281666001

children

Family history of 5,10 methylenetetrahydrofolate reductase deficiency 29810001000004100
Family history of alpha-1-antitrypsin deficiency 431912005
Family history of anencephaly 160418004
Family history of asplenia 3470001000004103
Family history of chromosomal anomaly 160425006
Family history of cleft lip 429954004
Family history of cleft palate 430086009
Family history of congenital anomaly of ear 64681000119102
Family history of congenital cataract 429977004
Family history of congenital hydrocephalus 63941000119102
Family history of congenital immunodeficiency disease 50050161000188101
Family history of congenital microcephaly 1148759006
Family history of congenital sensorineural hearing loss 456531000124109
Family history of cystic hygroma 64911000119103
Family history of dysmorphism 456671000124106
Family history of gastroschisis 6780001000004107
Family history of glycogen storage disease 64251000119106
Family history of hemoglobinopathy E 64391000119106
Family history of lysosomal storage disease 64171000119108
Family history of multiple congenital anomalies 64731000119106
Family history of neurofibromatosis 65021000119105
Family history of phenylketonuria 64161000119102
Family history of single congenital anomaly 85951000119104
Family history of tuberous sclerosis 417001009
Family history of Von Hippel-Lindau syndrome 64971000119106
FH: Cong. orthopedic anomaly 160424005
FH: Congenital anomaly NOS 160426007 removed: 2010-01-31
FH: Congenital CVS anomaly 266908007
FH: Congenital GIT anomaly 160422009
FH: Congenital GU anomaly 160423004
FH: Congenital RS anomaly 160421002
FH: Polycystic kidney 160389004
FH: Sickle cell anemia 160320002
FH: Sickle cell trait 160321003
FH: Thalassemia 160319008

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Context-dependent categories 243796009
Finding with explicit context 413350009
Family history of clinical finding 416471007
Family history of disorder 281666001
Family history of congenital disease 160417009

ancestors

sorted most to least specific

Family history of disorder 281666001
Family history of clinical finding 416471007
Finding with explicit context 413350009
Family history of 57177007
Context-dependent categories 243796009
SNOMED CT Concept 138875005

cpt crosswalks

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SNOMED CT Concept 138875005

Context-dependent categories 243796009

Finding with explicit context 413350009

Family history of clinical finding 416471007

Family history of disorder 281666001

Family history of congenital disease 160417009

SNOMED CT code