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724066002: Polysyndactyly and cardiac malformation 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
3429754015 Polysyndactyly and cardiac malformation syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3429755019 Polysyndactyly and cardiac malformation syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3429756018 Bonneau syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403208014 A rare, life-threatening developmental defect during embryogenesis characterized by polysyndactyly of fingers and toes as well as complex congenital heart defects (e.g. atrioventricular septal defects, aortic dextroposition, single ventricle, hypo- or hypertrophy of one side of the heart). Additional features may include dysmorphic traits (large fontanel, high forehead, ptosis, hypertelorism, epicanthus, low-set malformed ears, prominent root of the nose, bulbous nose, anteverted nares, long and smooth philtrum, thin upper lip, micrognathism, hirsutism, single transverse crease) nail hypoplasia, phalange agenesis/hypoplasia, flexion contractures, polysplenia, multiple hepatic/renal cysts, atrophic biliary vesicle, ductal plate malformation and genital anomalies (e.g. micropenis, undescended testes, hypoplastic scrotum). The syndrome is usually fatal in utero or in infancy, but survival cases have been reported. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403209018 A rare, life-threatening developmental defect during embryogenesis characterised by polysyndactyly of fingers and toes as well as complex congenital heart defects (e.g. atrioventricular septal defects, aortic dextroposition, single ventricle, hypo- or hypertrophy of one side of the heart). Additional features may include dysmorphic traits (large fontanel, high forehead, ptosis, hypertelorism, epicanthus, low-set malformed ears, prominent root of the nose, bulbous nose, anteverted nares, long and smooth philtrum, thin upper lip, micrognathism, hirsutism, single transverse crease) nail hypoplasia, phalange agenesis/hypoplasia, flexion contractures, polysplenia, multiple hepatic/renal cysts, atrophic biliary vesicle, ductal plate malformation and genital anomalies (e.g. micropenis, undescended testes, hypoplastic scrotum). The syndrome is usually fatal in utero or in infancy, but survival cases have been reported. 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
Polysyndactyly and cardiac malformation syndrome (disorder) Is a Congenital heart disease true Inferred relationship Some
Polysyndactyly and cardiac malformation syndrome (disorder) Is a Multiple system malformation syndrome true Inferred relationship Some
Polysyndactyly and cardiac malformation syndrome (disorder) Is a Polysyndactyly (disorder) true Inferred relationship Some
Polysyndactyly and cardiac malformation syndrome (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Polysyndactyly and cardiac malformation syndrome (disorder) Is a Cardiovascular system hereditary disorder true Inferred relationship Some
Polysyndactyly and cardiac malformation syndrome (disorder) Associated morphology Developmental anomaly false Inferred relationship Some 2
Polysyndactyly and cardiac malformation syndrome (disorder) Occurrence Congenital true Inferred relationship Some 2
Polysyndactyly and cardiac malformation syndrome (disorder) Finding site Heart structure false Inferred relationship Some 2
Polysyndactyly and cardiac malformation syndrome (disorder) Associated morphology Congenital abnormal fusion false Inferred relationship Some 3
Polysyndactyly and cardiac malformation syndrome (disorder) Occurrence Congenital true Inferred relationship Some 3
Polysyndactyly and cardiac malformation syndrome (disorder) Finding site Digit structure true Inferred relationship Some 3
Polysyndactyly and cardiac malformation syndrome (disorder) Associated morphology Congenital abnormal fusion false Inferred relationship Some 2
Polysyndactyly and cardiac malformation syndrome (disorder) Finding site Digit structure true Inferred relationship Some 2
Polysyndactyly and cardiac malformation syndrome (disorder) Associated morphology Supernumerary structure false Inferred relationship Some 1
Polysyndactyly and cardiac malformation syndrome (disorder) Occurrence Congenital true Inferred relationship Some 1
Polysyndactyly and cardiac malformation syndrome (disorder) Finding site Digit structure false Inferred relationship Some 1
Polysyndactyly and cardiac malformation syndrome (disorder) Associated morphology Supernumerary structure true Inferred relationship Some 3
Polysyndactyly and cardiac malformation syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3
Polysyndactyly and cardiac malformation syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Polysyndactyly and cardiac malformation syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Polysyndactyly and cardiac malformation syndrome (disorder) Finding site Heart structure true Inferred relationship Some 1
Polysyndactyly and cardiac malformation syndrome (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 1
Polysyndactyly and cardiac malformation syndrome (disorder) Is a Developmental hereditary disorder true Inferred relationship Some
Polysyndactyly and cardiac malformation syndrome (disorder) Associated morphology Abnormally fused structure (morphologic abnormality) true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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