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715648002: Skin structure of epicanthus inversus (body structure)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3303289017 Skin structure of epicanthus inversus (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303290014 Skin structure of epicanthus inversus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Skin structure of epicanthus inversus (body structure) Is a Skin structure of lower eyelid true Inferred relationship Some
Skin structure of epicanthus inversus (body structure) Is a Skin structure of epicanthal fold (body structure) true Inferred relationship Some
Skin structure of epicanthus inversus (body structure) Laterality Side (qualifier value) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Skin of eyelid fold arises in the lower eyelid tarsal region and extends up through the medial canthus towards the brow. Is a True Skin structure of epicanthus inversus (body structure) Inferred relationship Some
Epicanthus inversus (finding) Finding site True Skin structure of epicanthus inversus (body structure) Inferred relationship Some 1
A rare ophthalmic disorder characterized by blepharophimosis, ptosis, epicanthus inversus, and telecanthus, that can appear associated with (type 1) or without primary ovarian insufficiency (POI; type 2). Finding site False Skin structure of epicanthus inversus (body structure) Inferred relationship Some 1
A rare disorder of the ocular adnexa characterized by an extended phenotype of blepharophimosis, ptosis, epicanthus inversus and telecanthus syndrome (BPES). When BPES is caused by a microdeletion encompassing other genes in addition to the causative gene FOXL2, the patient has additional features including intellectual disability, external genital anomaly, spastic diplegia, and speech delay. Acquired microcephaly can also be observed. Finding site True Skin structure of epicanthus inversus (body structure) Inferred relationship Some 3
A rare ophthalmic disorder characterized by blepharophimosis, ptosis, epicanthus inversus, and telecanthus, that can appear associated with (type 1) or without primary ovarian insufficiency (POI; type 2). Finding site True Skin structure of epicanthus inversus (body structure) Inferred relationship Some 3

Reference Sets

Lateralizable body structure reference set (foundation metadata concept)

Anatomy structure and entire association reference set (foundation metadata concept)

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