Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome 721977007

SNOMED CT code

SNOMED code

721977007

name

Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome

status

active

date introduced

2017-01-31

fully specified name(s)

Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome (disorder)

synonyms

Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome

attributes - group2

Occurrence

Congenital 255399007

Pathological process

Pathological developmental process 308490002

Associated morphology

Fibrosis 112674009

Finding site

Lung structure 39607008

attributes - group3

Pathological process

Pathological developmental process 308490002

Associated morphology

Morphologically abnormal structure 49755003

Occurrence

Congenital 255399007

Finding site

Ovarian endocrine structure 304043001

attributes - group4

Pathological process

Abnormal immune process 769247005

attributes - group1

Has interpretation

Decreased 1250004

Interprets

Hormone secretion 60877009

parents

Autosomal recessive SCID (severe combined immunodeficiency disease) 362993009
Developmental hereditary disorder 363070008
Hereditary disorder of endocrine system 363104002
Reproductive system hereditary disorder 363290007
Congenital anomaly of lung 47147007
Fibrosis of lung 51615001
Pure gonadal dysgenesis 46,XX 95198001

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Congenital disease 66091009
Congenital immunodeficiency disease 36138009
Severe combined immunodeficiency disease 31323000
Autosomal recessive SCID (severe combined immunodeficiency disease) 362993009
Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome 721977007

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Developmental disorder 5294002
Developmental hereditary disorder 363070008
Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome 721977007

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Disorder of body system 362965005
Disorder of endocrine system 362969004
Hereditary disorder of endocrine system 363104002
Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome 721977007

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Disorder of body system 362965005
Hereditary disorder by system 363137000
Reproductive system hereditary disorder 363290007
Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome 721977007

SNOMED CT Concept 138875005
Clinical finding 404684003
Respiratory finding 106048009
Lower respiratory tract finding 301226008
Congenital anomaly of lower respiratory system 123654008
Congenital anomaly of lung 47147007
Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome 721977007

SNOMED CT Concept 138875005
Clinical finding 404684003
Viscus structure finding 406123005
Lung finding 301230006
Disorder of lung 19829001
Lesion of lung 301232003
Fibrosis of lung 51615001
Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome 721977007

SNOMED CT Concept 138875005
Clinical finding 404684003
Endocrine finding 106176003
Decreased hormone secretion 42497006
Ovarian failure 111550004
Primary ovarian failure 65846009
Ovarian dysgenesis 205683001
Pure gonadal dysgenesis 46,XX 95198001
Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome 721977007

ancestors

sorted most to least specific

Autosomal recessive SCID (severe combined immunodeficiency disease) 362993009
Developmental hereditary disorder 363070008
Hereditary disorder of endocrine system 363104002
Reproductive system hereditary disorder 363290007
Congenital anomaly of lung 47147007
Fibrosis of lung 51615001
Pure gonadal dysgenesis 46,XX 95198001
Severe combined immunodeficiency disease 31323000
Congenital anomaly of lower respiratory system 123654008
Lesion of lung 301232003
Ovarian dysgenesis 205683001
Autosomal recessive hereditary disorder 85995004
Congenital anomaly of thorax 363035006
Pure gonadal dysgenesis 95219002
Congenital immunodeficiency disease 36138009
Disorder of lung 19829001
Congenital anomaly of endocrine ovary 370966000
Autosomal hereditary disorder 1899006
Hereditary disorder of immune system 363138005
Combined immunodeficiency disease 442459007
Congenital malformation of the respiratory system 275260000
Primary ovarian failure 65846009
Congenital anomaly of upper trunk 363037003
Disorder of lower respiratory system 128272009
Disorder of thorax 118946009
Hereditary disorder by system 363137000
Primary immune deficiency disorder 58606001
Lung finding 301230006
Ovarian failure 111550004
Congenital anomaly of endocrine gonad 371118004
Congenital anomaly of ovary 38296007
Primary hypogonadism 370999003
Immunodeficiency disorder 234532001
Hereditary disease 32895009
Disorder of respiratory system 50043002
Finding of region of thorax 298705000
Lower respiratory tract finding 301226008
Disorder of thoracic segment of trunk 609622007
Gonadal dysgenesis 205681004
Female hypogonadism syndrome 16041008
Decreased hormone secretion 42497006
Congenital anomaly of endocrine gland 4184009
Congenital anomaly of abdomen 363024001
Congenital anomaly of the pelvis 47583008
Congenital anomaly of female genital system 59035004
Disorder of immune function 414029004
Genetic disease 782964007
Respiratory finding 106048009
Finding of upper trunk 609623002
Disorder of endocrine ovary 37102008
Congenital malformation of genital organs 204821009
Hypogonadism 48130008
Endocrine finding 106176003
Decline in functional status 154091000119106
Congenital female urogenital anomaly 428680008
Disorder of endocrine gonad 127345001
Genitourinary congenital anomalies 287085006
Disorder of ovary 5552004
Functional finding 118228005
Disorder of endocrine system 362969004
Congenital anomaly of lower trunk 363030001
Disorder of abdomen 118948005
Disorder of female genital organs 244938009
Ovary finding 289834006
Disorder of female genital system 310789003
Disorder of pelvis 609620004
Congenital abnormality of lower limb and pelvic girdle 253937004
Congenital anomaly of trunk 78626001
Female reproductive system disorder 363124003
Pelvic organ finding 700006000
Disorder of reproductive system 362968007
Congenital malformation 276654001
Female genitalia finding 248842004
Disorder of pelvic region of trunk 609619005
Abdominal organ finding 249561001
Finding of pelvis 609626005
Disorder of the genitourinary system 42030000
Genital finding 300479008
Congenital disease 66091009
Developmental disorder 5294002
Finding of abdomen 609624008
Viscus structure finding 406123005
Finding of pelvic region of trunk 609625009
Disorder of body system 362965005
Urogenital finding 118238000
Disorder of abdominopelvic segment of trunk 822988000
Finding of abdominopelvic segment of trunk 822987005
Disorder of trunk 128121009
Disease 64572001
Finding of trunk structure 302292003
Clinical finding 404684003
SNOMED CT Concept 138875005

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SNOMED CT Concept 138875005

Clinical finding 404684003

Disease 64572001

Congenital disease 66091009

Congenital immunodeficiency disease 36138009

Severe combined immunodeficiency disease 31323000

Autosomal recessive SCID (severe combined immunodeficiency disease) 362993009

Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome 721977007

SNOMED CT code