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732263008: Melhem Fahl syndrome (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3465122014 Melhem Fahl syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3465123016 Melhem Fahl syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3465124010 Syndrome that was described in two siblings born to consanguineous parents in 1985 with the presence of 15 dorsal vertebrae and rib pairs. No other cases have been documented since the initial report. 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
Melhem Fahl syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Melhem Fahl syndrome (disorder) morphologie associée (attribut) dysplasie true Inferred relationship Some 1
Melhem Fahl syndrome (disorder) est un(e) (attribut) Dysostosis true Inferred relationship Some
Melhem Fahl syndrome (disorder) morphologie associée (attribut) Congenital dysplasia false Inferred relationship Some 1
Melhem Fahl syndrome (disorder) survenue (attribut) congénital true Inferred relationship Some 1
Melhem Fahl syndrome (disorder) localisation d'une constatation (attribut) structure osseuse true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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