FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

723998001: Short stature, Pierre Robin sequence, cleft mandible, hand anomalies, clubfoot 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
3498174017 Robin sequence with cleft mandible and limb anomalies syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3498175016 Short stature, Pierre Robin sequence, cleft mandible, hand anomalies, clubfoot syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3498176015 Short stature, Pierre Robin sequence, cleft mandible, hand anomalies, clubfoot syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3498177012 Richieri Costa Pereira syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403189010 Richieri Costa-Pereira syndrome is characterized by short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies (including hypoplastic thumbs), and clubfoot. It has been described in 14 Brazilian families and in one unrelated French patient. Prominent low set ears and a highly arched palate were also observed. Transmission is autosomal recessive. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403190018 Richieri Costa-Pereira syndrome is characterised by short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies (including hypoplastic thumbs), and clubfoot. It has been described in 14 Brazilian families and in one unrelated French patient. Prominent low set ears and a highly arched palate were also observed. Transmission is autosomal recessive. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3498174017 Robin sequence with cleft mandible and limb anomalies syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3498175016 Short stature, Pierre Robin sequence, cleft mandible, hand anomalies, clubfoot syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3498176015 Short stature, Pierre Robin sequence, cleft mandible, hand anomalies, clubfoot syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3498177012 Richieri Costa Pereira syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3499906011 Syndrome with characteristics of short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies (including hypoplastic thumbs) and clubfoot. It has been described in 14 Brazilian families and in one unrelated French patient. Prominent low set ears and highly arched palate was also observed. Transmission is autosomal recessive. There is evidence this syndrome is caused by homozygous or compound heterozygous mutation in the EIF4A3 gene on chromosome 17q25. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403189010 Richieri Costa-Pereira syndrome is characterized by short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies (including hypoplastic thumbs), and clubfoot. It has been described in 14 Brazilian families and in one unrelated French patient. Prominent low set ears and a highly arched palate were also observed. Transmission is autosomal recessive. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403190018 Richieri Costa-Pereira syndrome is characterised by short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies (including hypoplastic thumbs), and clubfoot. It has been described in 14 Brazilian families and in one unrelated French patient. Prominent low set ears and a highly arched palate were also observed. Transmission is autosomal recessive. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3385871001000114 Richieri-Costa-Pereira-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3385871001000114 Richieri-Costa-Pereira-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Short stature, Pierre Robin sequence, cleft mandible, hand anomalies, clubfoot syndrome Is a Robin sequence true Inferred relationship Existential restriction modifier (core metadata concept)
Short stature, Pierre Robin sequence, cleft mandible, hand anomalies, clubfoot syndrome Is a Multiple malformation syndrome with facial-limb defects as major feature true Inferred relationship Existential restriction modifier (core metadata concept)
Short stature, Pierre Robin sequence, cleft mandible, hand anomalies, clubfoot syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Short stature, Pierre Robin sequence, cleft mandible, hand anomalies, clubfoot syndrome Is a Cleft mandible (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Short stature, Pierre Robin sequence, cleft mandible, hand anomalies, clubfoot syndrome Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Short stature, Pierre Robin sequence, cleft mandible, hand anomalies, clubfoot syndrome Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier (core metadata concept)
Short stature, Pierre Robin sequence, cleft mandible, hand anomalies, clubfoot syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Short stature, Pierre Robin sequence, cleft mandible, hand anomalies, clubfoot syndrome Finding site Limb structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Short stature, Pierre Robin sequence, cleft mandible, hand anomalies, clubfoot syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Short stature, Pierre Robin sequence, cleft mandible, hand anomalies, clubfoot syndrome Finding site Bone structure of mandible false Inferred relationship Existential restriction modifier (core metadata concept) 2
Short stature, Pierre Robin sequence, cleft mandible, hand anomalies, clubfoot syndrome Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 3
Short stature, Pierre Robin sequence, cleft mandible, hand anomalies, clubfoot syndrome Finding site Limb structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Short stature, Pierre Robin sequence, cleft mandible, hand anomalies, clubfoot syndrome Associated morphology Developmental failure of fusion (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Short stature, Pierre Robin sequence, cleft mandible, hand anomalies, clubfoot syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Short stature, Pierre Robin sequence, cleft mandible, hand anomalies, clubfoot syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Short stature, Pierre Robin sequence, cleft mandible, hand anomalies, clubfoot syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Short stature, Pierre Robin sequence, cleft mandible, hand anomalies, clubfoot syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Short stature, Pierre Robin sequence, cleft mandible, hand anomalies, clubfoot syndrome Finding site Bone structure of mandible true Inferred relationship Existential restriction modifier (core metadata concept) 1
Short stature, Pierre Robin sequence, cleft mandible, hand anomalies, clubfoot syndrome Associated morphology Developmental failure of fusion (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Short stature, Pierre Robin sequence, cleft mandible, hand anomalies, clubfoot syndrome Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Short stature, Pierre Robin sequence, cleft mandible, hand anomalies, clubfoot syndrome Finding site Face structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 3
Short stature, Pierre Robin sequence, cleft mandible, hand anomalies, clubfoot syndrome Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 3
Short stature, Pierre Robin sequence, cleft mandible, hand anomalies, clubfoot syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

Back to Start