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722280000: Ackerman 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
3331413017 Ackerman syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3331414011 Ackerman syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3331415012 Ackerman syndrome has characteristics of pyramidal molar roots and taurodontism associated with variable anomalies. It has been described in two generations of one family. Both parents and their six siblings had pyramidal, taurodont or fused molar roots. Some of the patients also had hypotrichosis, an abnormal upper lip, thickened and wide philtrum, and/or juvenile glaucoma. Other features included entropion of the eyelid, syndactyly and clinodactyly of the fifth fingers. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
11389781000172110 syndrome de molaires pyramidales et lèvre supérieure anormale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
11389791000172113 syndrome d'Ackerman fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
11389801000172114 syndrome de molaires avec racines fusionnées d'Ackerman fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
4656941000172119 Ackerman-gefuseerde-kieswortels-syndroom nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) Belgian module (core metadata concept)
4656951000172117 piramidale molaren-abnormale bovenlip-syndroom nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
4656961000172115 syndroom van piramidale molaren en abnormale bovenlip nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Ackerman syndrome (disorder) Is a Ectodermal dysplasia true Inferred relationship Some
Ackerman syndrome (disorder) Is a Multiple system malformation syndrome true Inferred relationship Some
Ackerman syndrome (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Ackerman syndrome (disorder) Is a Digestive system hereditary disorder (disorder) false Inferred relationship Some
Ackerman syndrome (disorder) Is a Hereditary disorder of the integument true Inferred relationship Some
Ackerman syndrome (disorder) Is a Congenital anomaly of tooth (disorder) true Inferred relationship Some
Ackerman syndrome (disorder) Occurrence Congenital true Inferred relationship Some 3
Ackerman syndrome (disorder) Associated morphology Developmental anomaly false Inferred relationship Some 4
Ackerman syndrome (disorder) Occurrence Congenital false Inferred relationship Some 4
Ackerman syndrome (disorder) Finding site Skin structure false Inferred relationship Some 4
Ackerman syndrome (disorder) Occurrence Congenital false Inferred relationship Some 5
Ackerman syndrome (disorder) Associated morphology Developmental anomaly false Inferred relationship Some 5
Ackerman syndrome (disorder) Associated morphology Congenital dysplasia false Inferred relationship Some 3
Ackerman syndrome (disorder) Finding site Ectoderm structure false Inferred relationship Some 3
Ackerman syndrome (disorder) Finding site Skin structure true Inferred relationship Some 3
Ackerman syndrome (disorder) Finding site Tooth structure false Inferred relationship Some 5
Ackerman syndrome (disorder) Occurrence Congenital true Inferred relationship Some 2
Ackerman syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Ackerman syndrome (disorder) Occurrence Congenital true Inferred relationship Some 1
Ackerman syndrome (disorder) Finding site Ectoderm structure true Inferred relationship Some 2
Ackerman syndrome (disorder) Associated morphology Congenital dysplasia false Inferred relationship Some 2
Ackerman syndrome (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 3
Ackerman syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Ackerman syndrome (disorder) Finding site Tooth structure true Inferred relationship Some 1
Ackerman syndrome (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 1
Ackerman syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3
Ackerman syndrome (disorder) Associated morphology Dysplasia true Inferred relationship Some 2
Ackerman syndrome (disorder) Is a Developmental hereditary disorder true Inferred relationship Some
Ackerman syndrome (disorder) Is a Hereditary disorder of tooth true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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