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720496006: Anophthalmia plus syndrome (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3321023011 Anophthalmia plus syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3321024017 Anophthalmia plus syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3321025016 Fryns microphthalmia syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3321026015 A very rare multiple congenital anomaly syndrome with characteristics of anophthalmia or severe microphthalmia, cleft lip/palate, facial cleft and sacral neural tube defects, along with various additional anomalies including congenital glaucoma, iris coloboma, primary hyperplastic vitreous, hypertelorism, low-set ears, clinodactyly, choanal atresia/stenosis, dysgenesis of sacrum, tethering of spinal cord, syringomyelia, hypoplasia of corpus callosum, cerebral ventriculomegaly and endocrine abnormalities. An autosomal recessive inheritance has been suggested. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Anophthalmia plus syndrome (disorder) Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Some
Anophthalmia plus syndrome (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Anophthalmia plus syndrome (disorder) Is a Agenesis of eye false Inferred relationship Some
Anophthalmia plus syndrome (disorder) Is a Hereditary disorder of the visual system (disorder) true Inferred relationship Some
Anophthalmia plus syndrome (disorder) Associated morphology Congenital absence (morphologic abnormality) false Inferred relationship Some 2
Anophthalmia plus syndrome (disorder) Occurrence Congenital true Inferred relationship Some 2
Anophthalmia plus syndrome (disorder) Finding site Entire eye false Inferred relationship Some 2
Anophthalmia plus syndrome (disorder) Occurrence Congenital false Inferred relationship Some 3
Anophthalmia plus syndrome (disorder) Associated morphology Developmental anomaly false Inferred relationship Some 2
Anophthalmia plus syndrome (disorder) Finding site Face structure false Inferred relationship Some 2
Anophthalmia plus syndrome (disorder) Associated morphology Congenital absence (morphologic abnormality) false Inferred relationship Some 3
Anophthalmia plus syndrome (disorder) Finding site Entire eye false Inferred relationship Some 3
Anophthalmia plus syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Anophthalmia plus syndrome (disorder) Finding site Face structure true Inferred relationship Some 1
Anophthalmia plus syndrome (disorder) Occurrence Congenital true Inferred relationship Some 1
Anophthalmia plus syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Anophthalmia plus syndrome (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 1
Anophthalmia plus syndrome (disorder) Is a Congenital anomaly of eye true Inferred relationship Some
Anophthalmia plus syndrome (disorder) Is a Developmental hereditary disorder true Inferred relationship Some
Anophthalmia plus syndrome (disorder) Associated morphology Absence (morphologic abnormality) true Inferred relationship Some 2
Anophthalmia plus syndrome (disorder) Finding site Entire eye proper true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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