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1234831009: Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2022. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
5084176012 MIRAGE (myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy) syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
5084177015 Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
5084178013 Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
5084179017 Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital phenotypes, enteropathy syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
5084180019 MIRAGE syndrome en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy syndrome Is a Adrenogenital disorder true Inferred relationship Existential restriction modifier
Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy syndrome Is a Hereditary disorder of endocrine system true Inferred relationship Existential restriction modifier
Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy syndrome Is a Reproductive system hereditary disorder true Inferred relationship Existential restriction modifier
Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy syndrome Is a Short stature co-occurrent and due to endocrine disorder true Inferred relationship Existential restriction modifier
Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy syndrome Is a 46,XY disorder of sex development true Inferred relationship Existential restriction modifier
Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy syndrome Is a Congenital hypoplasia of adrenal gland true Inferred relationship Existential restriction modifier
Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy syndrome Due to Disorder of endocrine system true Inferred relationship Existential restriction modifier 3
Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy syndrome Finding site Genital structure true Inferred relationship Existential restriction modifier 1
Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy syndrome Finding site Adrenal cortex structure true Inferred relationship Existential restriction modifier 2
Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy syndrome Associated morphology Hypoplasia true Inferred relationship Existential restriction modifier 2
Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy syndrome Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier
Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy syndrome Interprets Body height measure true Inferred relationship Existential restriction modifier 4
Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy syndrome Has interpretation Below reference range true Inferred relationship Existential restriction modifier 4

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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