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721879006: Microphthalmia with linear skin defect syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3326425013 Microphthalmia with linear skin defect syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3326426014 Microphthalmia with linear skin defect syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3326427017 Syndromic microphthalmia type 7 en Synonym Active Entire term case insensitive SNOMED CT core module
3326428010 MIDAS syndrome (microphthalmia, dermal aplasia, sclerocornea) syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3326429019 MIDAS 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
Microphthalmia with linear skin defect syndrome Is a Microphthalmos true Inferred relationship Existential restriction modifier
Microphthalmia with linear skin defect syndrome Is a X-linked hereditary disease false Inferred relationship Existential restriction modifier
Microphthalmia with linear skin defect syndrome Is a Congenital anomaly of skin true Inferred relationship Existential restriction modifier
Microphthalmia with linear skin defect syndrome Is a Hereditary disorder of the integument true Inferred relationship Existential restriction modifier
Microphthalmia with linear skin defect syndrome Is a Hereditary disorder of the visual system true Inferred relationship Existential restriction modifier
Microphthalmia with linear skin defect syndrome Associated morphology Congenital smallness true Inferred relationship Existential restriction modifier 2
Microphthalmia with linear skin defect syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Microphthalmia with linear skin defect syndrome Finding site Entire eye true Inferred relationship Existential restriction modifier 2
Microphthalmia with linear skin defect syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Microphthalmia with linear skin defect syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Microphthalmia with linear skin defect syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Microphthalmia with linear skin defect syndrome Associated morphology Congenital smallness false Inferred relationship Existential restriction modifier 3
Microphthalmia with linear skin defect syndrome Finding site Entire eye false Inferred relationship Existential restriction modifier 3
Microphthalmia with linear skin defect syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Microphthalmia with linear skin defect syndrome Finding site Skin structure true Inferred relationship Existential restriction modifier 1
Microphthalmia with linear skin defect syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Microphthalmia with linear skin defect syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Microphthalmia with linear skin defect syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Microphthalmia with linear skin defect syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Microphthalmia with linear skin defect syndrome Is a X-linked dominant hereditary disease true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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