715440003: Mirror hands and feet co-occurrent with nasal defect (disorder)

• SNOMED CT Concept\Clinical finding (finding)\...
• \Head finding (finding)\Finding of head region\Finding of face\Disorder of face (disorder)\Congenital anomaly of face (disorder)\Congenital anomaly of nose\Mirror hands and feet co-occurrent with nasal defect
• \Head finding (finding)\Finding of head region\Finding of face\Disorder of face (disorder)\Disorder of the nose\Congenital anomaly of nose\Mirror hands and feet co-occurrent with nasal defect
• \Head finding (finding)\Finding of head region\Finding of face\Nose finding\Disorder of the nose\Congenital anomaly of nose\Mirror hands and feet co-occurrent with nasal defect
• \Head finding (finding)\Finding of head region\Disorder of nose and nasopharynx\Congenital abnormality of nose and nasopharynx\Congenital anomaly of nose\Mirror hands and feet co-occurrent with nasal defect
• \Head finding (finding)\Finding of head region\Disorder of nose and nasopharynx\Disorder of the nose\Congenital anomaly of nose\Mirror hands and feet co-occurrent with nasal defect
• \Head finding (finding)\Disorder of head (disorder)\Disorder of nose and nasopharynx\Congenital abnormality of nose and nasopharynx\Congenital anomaly of nose\Mirror hands and feet co-occurrent with nasal defect
• \Head finding (finding)\Disorder of head (disorder)\Disorder of nose and nasopharynx\Disorder of the nose\Congenital anomaly of nose\Mirror hands and feet co-occurrent with nasal defect
• \Head finding (finding)\Disorder of head (disorder)\Disorder of face (disorder)\Congenital anomaly of face (disorder)\Congenital anomaly of nose\Mirror hands and feet co-occurrent with nasal defect
• \Head finding (finding)\Disorder of head (disorder)\Disorder of face (disorder)\Disorder of the nose\Congenital anomaly of nose\Mirror hands and feet co-occurrent with nasal defect
• \Head finding (finding)\Disorder of head (disorder)\Congenital anomaly of head\Congenital anomaly of face (disorder)\Congenital anomaly of nose\Mirror hands and feet co-occurrent with nasal defect
• \Head finding (finding)\Disorder of head (disorder)\Congenital anomaly of head\Congenital abnormality of nose and nasopharynx\Congenital anomaly of nose\Mirror hands and feet co-occurrent with nasal defect
• \Finding of limb structure (finding)\Disorder of limb\...
• \Disorder of digit\Congenital anomaly of digit\...
• \Syndactyly (disorder)\Polysyndactyly (disorder)\Mirror hands and feet co-occurrent with nasal defect
• \Polydactyly (disorder)\Polysyndactyly (disorder)\Mirror hands and feet co-occurrent with nasal defect
• \Congenital anomaly of limb\Congenital anomaly of digit\Syndactyly (disorder)\Polysyndactyly (disorder)\Mirror hands and feet co-occurrent with nasal defect
• \Congenital anomaly of limb\Congenital anomaly of digit\Polydactyly (disorder)\Polysyndactyly (disorder)\Mirror hands and feet co-occurrent with nasal defect
• \Congenital anomaly of limb\Polymelia\Polydactyly (disorder)\Polysyndactyly (disorder)\Mirror hands and feet co-occurrent with nasal defect
• \Ear, nose and throat finding\affection de l'oreille, du nez et de la gorge\Disorder of the nose\Congenital anomaly of nose\Mirror hands and feet co-occurrent with nasal defect
• \Ear, nose and throat finding\Nose finding\Disorder of the nose\Congenital anomaly of nose\Mirror hands and feet co-occurrent with nasal defect
• \Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Mirror hands and feet co-occurrent with nasal defect
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Mirror hands and feet co-occurrent with nasal defect
• \Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with limb defect as major feature\Mirror hands and feet co-occurrent with nasal defect
• \Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital anomaly of head\Congenital anomaly of face (disorder)\Congenital anomaly of nose\Mirror hands and feet co-occurrent with nasal defect
• \Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital anomaly of head\Congenital abnormality of nose and nasopharynx\Congenital anomaly of nose\Mirror hands and feet co-occurrent with nasal defect
• \Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital anomaly of limb\Congenital anomaly of digit\Syndactyly (disorder)\Polysyndactyly (disorder)\Mirror hands and feet co-occurrent with nasal defect
• \Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital anomaly of limb\Congenital anomaly of digit\Polydactyly (disorder)\Polysyndactyly (disorder)\Mirror hands and feet co-occurrent with nasal defect
• \Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital anomaly of limb\Polymelia\Polydactyly (disorder)\Polysyndactyly (disorder)\Mirror hands and feet co-occurrent with nasal defect
• \Disease\affection de l'oreille, du nez et de la gorge\Disorder of the nose\Congenital anomaly of nose\Mirror hands and feet co-occurrent with nasal defect
• \Disease\Disorder of limb\Disorder of digit\Congenital anomaly of digit\Syndactyly (disorder)\Polysyndactyly (disorder)\Mirror hands and feet co-occurrent with nasal defect
• \Disease\Disorder of limb\Disorder of digit\Congenital anomaly of digit\Polydactyly (disorder)\Polysyndactyly (disorder)\Mirror hands and feet co-occurrent with nasal defect
• \Disease\Disorder of limb\Congenital anomaly of limb\Congenital anomaly of digit\Syndactyly (disorder)\Polysyndactyly (disorder)\Mirror hands and feet co-occurrent with nasal defect
• \Disease\Disorder of limb\Congenital anomaly of limb\Congenital anomaly of digit\Polydactyly (disorder)\Polysyndactyly (disorder)\Mirror hands and feet co-occurrent with nasal defect
• \Disease\Disorder of limb\Congenital anomaly of limb\Polymelia\Polydactyly (disorder)\Polysyndactyly (disorder)\Mirror hands and feet co-occurrent with nasal defect
• \Disease\Disorder of head (disorder)\Disorder of nose and nasopharynx\Congenital abnormality of nose and nasopharynx\Congenital anomaly of nose\Mirror hands and feet co-occurrent with nasal defect
• \Disease\Disorder of head (disorder)\Disorder of nose and nasopharynx\Disorder of the nose\Congenital anomaly of nose\Mirror hands and feet co-occurrent with nasal defect
• \Disease\Disorder of head (disorder)\Disorder of face (disorder)\Congenital anomaly of face (disorder)\Congenital anomaly of nose\Mirror hands and feet co-occurrent with nasal defect
• \Disease\Disorder of head (disorder)\Disorder of face (disorder)\Disorder of the nose\Congenital anomaly of nose\Mirror hands and feet co-occurrent with nasal defect
• \Disease\Disorder of head (disorder)\Congenital anomaly of head\Congenital anomaly of face (disorder)\Congenital anomaly of nose\Mirror hands and feet co-occurrent with nasal defect
• \Disease\Disorder of head (disorder)\Congenital anomaly of head\Congenital abnormality of nose and nasopharynx\Congenital anomaly of nose\Mirror hands and feet co-occurrent with nasal defect
• \Disease\Developmental disorder (disorder)\Developmental hereditary disorder\Mirror hands and feet co-occurrent with nasal defect
• \Disease\Developmental disorder (disorder)\Congenital malformation\Congenital malformation syndrome\Multiple system malformation syndrome\Multiple malformation syndrome with limb defect as major feature\Mirror hands and feet co-occurrent with nasal defect
• \Disease\Developmental disorder (disorder)\Congenital malformation\Congenital anomaly of head\Congenital anomaly of face (disorder)\Congenital anomaly of nose\Mirror hands and feet co-occurrent with nasal defect
• \Disease\Developmental disorder (disorder)\Congenital malformation\Congenital anomaly of head\Congenital abnormality of nose and nasopharynx\Congenital anomaly of nose\Mirror hands and feet co-occurrent with nasal defect
• \Disease\Developmental disorder (disorder)\Congenital malformation\Congenital anomaly of limb\Congenital anomaly of digit\Syndactyly (disorder)\Polysyndactyly (disorder)\Mirror hands and feet co-occurrent with nasal defect
• \Disease\Developmental disorder (disorder)\Congenital malformation\Congenital anomaly of limb\Congenital anomaly of digit\Polydactyly (disorder)\Polysyndactyly (disorder)\Mirror hands and feet co-occurrent with nasal defect
• \Disease\Developmental disorder (disorder)\Congenital malformation\Congenital anomaly of limb\Polymelia\Polydactyly (disorder)\Polysyndactyly (disorder)\Mirror hands and feet co-occurrent with nasal defect

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
3302639010	Mirror hands and feet co-occurrent with nasal defect (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3302640012	Mirror hands and feet co-occurrent with nasal defect	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3302641011	Laurin Sandrow syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3302642016	Sandrow syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5400899015	Laurin-Sandrow syndrome (LSS) is characterized by complete polysyndactyly of the hands, mirror feet and nose anomalies (hypoplasia of the nasal alae and short columella), often associated with ulnar and/or fibular duplication (and sometimes tibial agenesis). It has been described in less than 20 cases. Some cases with the same clinical signs but without nasal defects have also been reported and may represent the same entity. The etiology of LSS is unknown. Different modes of inheritance have been suggested.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5400900013	Laurin-Sandrow syndrome (LSS) is characterised by complete polysyndactyly of the hands, mirror feet and nose anomalies (hypoplasia of the nasal alae and short columella), often associated with ulnar and/or fibular duplication (and sometimes tibial agenesis). It has been described in less than 20 cases. Some cases with the same clinical signs but without nasal defects have also been reported and may represent the same entity. The aetiology of LSS is unknown. Different modes of inheritance have been suggested.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3302639010	Mirror hands and feet co-occurrent with nasal defect (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3302640012	Mirror hands and feet co-occurrent with nasal defect	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3302640012	Mirror hands and feet co-occurrent with nasal defect	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3302641011	Laurin Sandrow syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3302642016	Sandrow syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3302643014	Complete polysyndactyly of the hands, mirror feet and nose anomalies (hypoplasia of the nasal alae and short columella), often associated with ulnar and/or fibular duplication (and sometimes tibial agenesis).	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5400899015	Laurin-Sandrow syndrome (LSS) is characterized by complete polysyndactyly of the hands, mirror feet and nose anomalies (hypoplasia of the nasal alae and short columella), often associated with ulnar and/or fibular duplication (and sometimes tibial agenesis). It has been described in less than 20 cases. Some cases with the same clinical signs but without nasal defects have also been reported and may represent the same entity. The etiology of LSS is unknown. Different modes of inheritance have been suggested.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5400900013	Laurin-Sandrow syndrome (LSS) is characterised by complete polysyndactyly of the hands, mirror feet and nose anomalies (hypoplasia of the nasal alae and short columella), often associated with ulnar and/or fibular duplication (and sometimes tibial agenesis). It has been described in less than 20 cases. Some cases with the same clinical signs but without nasal defects have also been reported and may represent the same entity. The aetiology of LSS is unknown. Different modes of inheritance have been suggested.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3392951001000118	Laurin-Sandrow-Syndrom	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3392951001000118	Laurin-Sandrow-Syndrom	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

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Component annotation with string value reference set (foundation metadata concept)

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