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1172683008: Microcephaly, congenital cataract, psoriasiform dermatitis syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 30-Sep 2021. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4635206014 Sterol-C4-methyl oxidase deficiency en Synonym Active Only initial character case insensitive SNOMED CT core module
4635208010 SMO (sterol-C4-methyl oxidase) deficiency en Synonym Active Entire term case sensitive SNOMED CT core module
4635211011 Microcephaly, congenital cataract, psoriasiform dermatitis syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
4635212016 Microcephaly, congenital cataract, psoriasiform dermatitis syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Microcephaly, congenital cataract, psoriasiform dermatitis syndrome Is a Microcephaly true Inferred relationship Existential restriction modifier
Microcephaly, congenital cataract, psoriasiform dermatitis syndrome Is a Disorder of cholesterol synthesis true Inferred relationship Existential restriction modifier
Microcephaly, congenital cataract, psoriasiform dermatitis syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Microcephaly, congenital cataract, psoriasiform dermatitis syndrome Is a Hereditary disorder of the integument true Inferred relationship Existential restriction modifier
Microcephaly, congenital cataract, psoriasiform dermatitis syndrome Is a Hereditary disorder of the visual system true Inferred relationship Existential restriction modifier
Microcephaly, congenital cataract, psoriasiform dermatitis syndrome Is a Inborn error of lipoprotein metabolism true Inferred relationship Existential restriction modifier
Microcephaly, congenital cataract, psoriasiform dermatitis syndrome Is a Psoriasiform dermatitis true Inferred relationship Existential restriction modifier
Microcephaly, congenital cataract, psoriasiform dermatitis syndrome Is a Congenital cataract true Inferred relationship Existential restriction modifier
Microcephaly, congenital cataract, psoriasiform dermatitis syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Microcephaly, congenital cataract, psoriasiform dermatitis syndrome Interprets Head circumference true Inferred relationship Existential restriction modifier 4
Microcephaly, congenital cataract, psoriasiform dermatitis syndrome Has interpretation Below reference range true Inferred relationship Existential restriction modifier 4
Microcephaly, congenital cataract, psoriasiform dermatitis syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Microcephaly, congenital cataract, psoriasiform dermatitis syndrome Finding site Structure of lens of eye true Inferred relationship Existential restriction modifier 1
Microcephaly, congenital cataract, psoriasiform dermatitis syndrome Associated morphology Abnormally opaque structure true Inferred relationship Existential restriction modifier 1
Microcephaly, congenital cataract, psoriasiform dermatitis syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Microcephaly, congenital cataract, psoriasiform dermatitis syndrome Finding site Skin structure true Inferred relationship Existential restriction modifier 2
Microcephaly, congenital cataract, psoriasiform dermatitis syndrome Associated morphology Psoriasiform rash true Inferred relationship Existential restriction modifier 2
Microcephaly, congenital cataract, psoriasiform dermatitis syndrome Finding site Skin structure true Inferred relationship Existential restriction modifier 3
Microcephaly, congenital cataract, psoriasiform dermatitis syndrome Associated morphology Inflammatory morphology true Inferred relationship Existential restriction modifier 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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