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72523005: X-linked ichthyosis with steryl-sulfatase deficiency (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
120467017 Sex-linked ichthyosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
200289014 X-linked ichthyosis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
200290017 X-linked ichthyosis with steryl-sulfatase deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
502147010 X-linked ichthyosis with steryl-sulphatase deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
812810018 X-linked ichthyosis with steryl-sulfatase deficiency (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
2002221000005114 Kønsbunden ichthyose med steryl-sulfatase-mangel da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
X-linked ichthyosis with steryl-sulphatase deficiency Is a Congenital ichthyosis of skin true Inferred relationship Some
X-linked ichthyosis with steryl-sulphatase deficiency Is a X-linked hereditary disease (disorder) false Inferred relationship Some
X-linked ichthyosis with steryl-sulphatase deficiency Is a Inborn error of metabolism true Inferred relationship Some
X-linked ichthyosis with steryl-sulphatase deficiency Is a Deficiency of steryl-sulfatase true Inferred relationship Some
X-linked ichthyosis with steryl-sulphatase deficiency Occurrence Congenital false Inferred relationship Some
X-linked ichthyosis with steryl-sulphatase deficiency Associated morphology Hyperkeratosis false Inferred relationship Some
X-linked ichthyosis with steryl-sulphatase deficiency Finding site Structure of skin region false Inferred relationship Some
X-linked ichthyosis with steryl-sulphatase deficiency Associated morphology kongenit anomali false Inferred relationship Some 1
X-linked ichthyosis with steryl-sulphatase deficiency Finding site Skin structure false Inferred relationship Some 1
X-linked ichthyosis with steryl-sulphatase deficiency Associated morphology kongenit anomali false Inferred relationship Some 1
X-linked ichthyosis with steryl-sulphatase deficiency Finding site Skin structure false Inferred relationship Some 1
X-linked ichthyosis with steryl-sulphatase deficiency Occurrence Congenital false Inferred relationship Some 2
X-linked ichthyosis with steryl-sulphatase deficiency Associated morphology dysgenese false Inferred relationship Some 2
X-linked ichthyosis with steryl-sulphatase deficiency Finding site Skin structure false Inferred relationship Some 2
X-linked ichthyosis with steryl-sulphatase deficiency Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
X-linked ichthyosis with steryl-sulphatase deficiency Occurrence Congenital true Inferred relationship Some 1
X-linked ichthyosis with steryl-sulphatase deficiency Associated morphology Hyperkeratosis true Inferred relationship Some 1
X-linked ichthyosis with steryl-sulphatase deficiency Has interpretation Abnormal true Inferred relationship Some 2
X-linked ichthyosis with steryl-sulphatase deficiency Interprets Keratinization true Inferred relationship Some 2
X-linked ichthyosis with steryl-sulphatase deficiency Finding site Entire skin true Inferred relationship Some 1
X-linked ichthyosis with steryl-sulphatase deficiency Is a X-linked recessive hereditary disease true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
A rare genetic skin disease belonging to the Mendelian Disorders of Cornification (MeDOC) characterized by a generally mild cutaneous desquamation in association with extracutaneous manifestations as part of a syndrome. Is a True X-linked ichthyosis with steryl-sulphatase deficiency Inferred relationship Some

This concept is not in any reference sets

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