Oligohydramnios sequence 41962002

SNOMED CT code

SNOMED code

41962002

name

Oligohydramnios sequence

status

active

date introduced

2002-01-31

fully specified name(s)

Oligohydramnios sequence (disorder)

synonyms

BRA - Bilateral renal agenesis
Potter's anomaly of the kidney
Bilateral congenital absence of kidneys
Oligohydramnios sequence
Potter syndrome
Renofacial syndrome
Renal agenesis syndrome
Congenital absence of kidneys syndrome

attributes - group2

Pathological process

Pathological developmental process 308490002

Finding site

Entire right kidney 362208000

Occurrence

Congenital 255399007

Associated morphology

Agenesis 782173000

attributes - group1

Pathological process

Pathological developmental process 308490002

Occurrence

Congenital 255399007

Associated morphology

Agenesis 782173000

Finding site

Entire left kidney 362209008

parents

Developmental hereditary disorder 363070008
Hereditary nephropathy 367591000119105
Left renal agenesis 762907005
Right renal agenesis 762908000
Autosomal recessive hereditary disorder 85995004

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Developmental disorder 5294002
Developmental hereditary disorder 363070008
Oligohydramnios sequence 41962002

SNOMED CT Concept 138875005
Clinical finding 404684003
Viscus structure finding 406123005
Abdominal organ finding 249561001
Kidney finding 249578005
Kidney disease 90708001
Hereditary nephropathy 367591000119105
Oligohydramnios sequence 41962002

SNOMED CT Concept 138875005
Clinical finding 404684003
Viscus structure finding 406123005
Abdominal organ finding 249561001
Kidney finding 249578005
Absent kidney 249582007
Renal agenesis 204942005
Left renal agenesis 762907005
Oligohydramnios sequence 41962002

SNOMED CT Concept 138875005
Clinical finding 404684003
Viscus structure finding 406123005
Abdominal organ finding 249561001
Kidney finding 249578005
Absent kidney 249582007
Renal agenesis 204942005
Right renal agenesis 762908000
Oligohydramnios sequence 41962002

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Genetic disease 782964007
Hereditary disease 32895009
Autosomal hereditary disorder 1899006
Autosomal recessive hereditary disorder 85995004
Oligohydramnios sequence 41962002

ancestors

sorted most to least specific

Developmental hereditary disorder 363070008
Hereditary nephropathy 367591000119105
Left renal agenesis 762907005
Right renal agenesis 762908000
Autosomal recessive hereditary disorder 85995004
Hereditary disorder of the urinary system 363338001
Renal agenesis 204942005
Autosomal hereditary disorder 1899006
Left kidney absent 443768001
Right kidney absent 443806007
Absent kidney 249582007
Hereditary disorder by system 363137000
Congenital anomaly of the kidney 44513007
Hereditary disease 32895009
Kidney disease 90708001
Congenital malformation of the urinary system 253859003
Congenital anomaly of abdomen 363024001
Genetic disease 782964007
Kidney finding 249578005
Disorder of kidney and/or ureter 443820000
Disorder of retroperitoneum 734045002
Genitourinary congenital anomalies 287085006
Disorder of the urinary system 128606002
Abdominal organ finding 249561001
Disorder of abdomen 118948005
Congenital anomaly of lower trunk 363030001
Urinary system finding 106098005
Disorder of the genitourinary system 42030000
Viscus structure finding 406123005
Finding of abdomen 609624008
Congenital abnormality of lower limb and pelvic girdle 253937004
Congenital anomaly of trunk 78626001
Urogenital finding 118238000
Disorder of body system 362965005
Disorder of abdominopelvic segment of trunk 822988000
Congenital malformation 276654001
Finding of abdominopelvic segment of trunk 822987005
Developmental disorder 5294002
Disorder of trunk 128121009
Congenital disease 66091009
Disease 64572001
Finding of trunk structure 302292003
Clinical finding 404684003
SNOMED CT Concept 138875005

cpt crosswalks

Rules-based maps relating CPT® codes to and from SNOMED CT® clinical concepts. Forward and backward mapping allows for easy transition between code sets. Map-A-Code crosswalk tool easily crosswalks multiple codes between the code sets.

Access to this feature is available in the following products:

CPT® to SNOMED Crosswalks

Thank you for choosing Find-A-Code, please Sign In to remove ads.

MY NEWSLETTERS

FEES

FACILITY

RISK ADJUSTMENT

SNOMED CT Concept 138875005

Clinical finding 404684003

Disease 64572001

Developmental disorder 5294002

Developmental hereditary disorder 363070008

Oligohydramnios sequence 41962002

SNOMED CT code