Q87.2
BillableCongenital malformation syndromes predom involving limbs
Congenital malformation syndromes predominantly involving limbs
Status
Billable / Specific
Parent Code
Q87Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Holt-Oram syndrome
- Klippel-Trenaunay-Weber syndrome
- Nail patella syndrome
- Rubinstein-Taybi syndrome
- Sirenomelia syndrome
- Thrombocytopenia with absent radius [TAR] syndrome
- VATER syndrome
Excludes 2
Conditions not included here, but the patient may have both
- inborn errors of metabolism (E70-E88)
Use Additional Code
Additional codes that should follow this code
- code(s) to identify all associated manifestations
Also Known As / Clinical Terms
SNOMED CT
- Ruvalcaba syndrome3073006
- Femoral facial syndrome13280000
- Femoral hypoplasia - unusual facies syndrome13280000
- Congenital cleft hand13624003
- Lobster claw hand13624003
- Lobster-claw hand13624003
- CHILD (congenital hemidysplasia, ichthyosiform erythroderma, limb defects) syndrome17608003
- CHILD syndrome17608003
- Congenital hemidysplasia with ichthyosiform erythroderma and limb defects syndrome17608003
- Trichorhinophalangeal syndrome18077009
- Atriodigital dysplasia type 119092004
- Heart-hand syndrome type 119092004
- Holt Oram syndrome19092004
- Holt-Oram syndrome19092004
- Hereditary osteo-onychodysplasia22199006
- Nail patella syndrome22199006
- Nail-patella syndrome22199006
- Onychoosteodysplasia22199006
- Turner Kieser syndrome22199006
- Multiple malformation syndrome with facial-limb defects as major feature23359005
- Lacrimo-auriculo-dento-digital syndrome23817003
- Levy-Hollister syndrome23817003
- Townes Brocks syndrome24750000
- Townes syndrome24750000
- VATER anomalad27742002
- VATER association27742002
- VATER syndrome27742002
- Vertebral anomalies/dysgenesis, anal atresia, tracheo-esophageal fistula, esophageal atresia, renal anomalies, radial dysplasia (VATER) association27742002
- Vertebral anomalies/dysgenesis, anal atresia, tracheo-esophageal fistula, esophageal atresia, renal anomalies, radial dysplasia association27742002
- Vertebral anomalies/dysgenesis, anal atresia, tracheo-oesophageal fistula, oesophageal atresia, renal anomalies, radial dysplasia (VATER) association27742002
- Vertebral anomalies/dysgenesis, anal atresia, tracheo-oesophageal fistula, oesophageal atresia, renal anomalies, radial dysplasia association27742002
- Congenital aplastic anaemia28975000
- Congenital aplastic anemia28975000
- Constitutional aplastic anaemia28975000
- Constitutional aplastic anemia28975000
- Hypoplastic anaemia - familial28975000
- Hypoplastic anemia - familial28975000
- Mesomelic dysplasia - Nievergelt type33979003
- Nievergelt syndrome33979003
- Nievergelt's syndrome33979003
- Nievergelt-Erb syndrome33979003
- Adams-Oliver syndrome34748004
- Congenital absence of skin on scalp with limb-reduction anomaly34748004
- Type 2 aplasia cutis34748004
- Nager acrofacial dysostosis syndrome35520007
- Nager syndrome35520007
- Preaxial acrofacial dysostosis35520007
- 4q partial monosomy syndrome37506004
- Chromosome 4q deletion syndrome37506004
- Mietens syndrome40291001
- Langer-Giedion syndrome41069008
- TRPS II - Trichorhinophalangeal syndrome II41069008
- Trichorhinophalangeal syndrome II41069008
- Trichorhinophalangeal syndrome with exostosis41069008
- Multiple malformation syndrome with limb defect as major feature41443008
- Multiple malformation syndrome, small stature, without skeletal dysplasia41483000
- Hypoplastic anaemia41614006
- Hypoplastic anemia41614006
- Rubinstein-Taybi syndrome45582004
- Waardenburg syndrome47434006
- Waardenburg's syndrome47434006
- Limb reduction-ichthyosis syndrome68551007
- Acrocephalosyndactyly type 570410008
- Acrocephalosyndactyly type V70410008
- Pfeiffer syndrome70410008
- Pfeiffer-type acrocephalosyndactyly70410008
- Aase Smith II syndrome71988008
- Aase syndrome71988008
- Blackfan-Diamond anaemia71988008
- Blackfan-Diamond anemia71988008
- Congenital hypoplastic anaemia Blackfan-Diamond type71988008
- Congenital hypoplastic anemia Blackfan-Diamond type71988008
- Congenital pure red cell aplasia71988008
- MHL - Mixed hearing loss77507001
- Mixed conductive AND sensorineural hearing loss77507001
- Mixed conductive and sensorineural deafness77507001
- Mixed deafness77507001
- Mixed hearing loss77507001
- Mixed type deafness77507001
- Acromesomelic dysplasia Grebe type77542002
- Grebe dysplasia77542002
- Grebe syndrome77542002
- Escobar syndrome80773006
- Acrocephalosyndactyly, type III83015004
- Saethre-Chotzen syndrome83015004
- Congenital gastric hypoplasia83714006
- Congenital microgastria83714006
- Congenital small stomach83714006
- Microgastria83714006
- Congenital absence of radius84918006
- Radial aplasia-thrombocytopenia syndrome85589009
- TAR - Thrombocytopenia with absent radius syndrome85589009
- TAR syndrome85589009
- Thrombocytopenia with absent radius syndrome85589009
- Thrombocytopenia-absent radii syndrome85589009
- Chronic constitutional pure red cell anaemia88854002
- Chronic constitutional pure red cell anemia88854002
- Chronic constitutional pure red cell aplasia88854002
- Congenital erythroid hypoplasia88854002
- Congenital hypoplastic anaemia88854002
- Congenital hypoplastic anemia88854002
- Congenital pure red cell anaemia88854002
- Congenital pure red cell anemia88854002
- Congenital red cell aplasia88854002
- Erythrogenesis imperfecta88854002
- Familial hypoplastic anaemia88854002
- Familial hypoplastic anemia88854002
- Congenital abnormal shape of fibula92910001
- Congenital misshapen fibula92910001
- Congenital abnormal shape of tibia92954007
- Congenital misshapen tibia92954007
- Congenital anomaly of caudal vertebra92998007
- Congenital hypoplasia of femur93255008
- Congenital short femur93255008
- Bilateral hearing loss95820000
- Interparietal craniosynostosis109418001
- Sagittal craniosynostosis109418001
- Sagittal synostosis109418001
- Scaphocephaly109418001
- Conductive hearing loss, bilateral194417009
- Sensorineural hearing loss of bilateral ears194424005
- Sensorineural hearing loss of both ears194424005
- Mixed conductive and sensorineural hearing loss, bilateral194429000
- Anal atresia204712000
- Aproctia204712000
- Atresia ani204712000
- Congenital atresia of anus204712000
- Congenital imperforate anus204712000
- Imperforate anus204712000
- Acrocephalopolysyndactyly205260006
- Amelia of upper limb205306000
- Congenital complete absence of upper limb205306000
- Transverse deficiency of arm, shoulder level205306000
- Brachymesophalangia205317004
- Brachydactyly of toes205346006
- Cleft foot205358006
- Lobster claw foot205358006
- Split foot205358006
- Duplication of lower limb bone205368001
- Amegakaryocytic thrombocytopenia234482009
- Klein-Waardenberg syndrome237918004
- Klein-Waardenberg's syndrome237918004
- Waardenburg syndrome type 3237918004
- Waardenburg syndrome type III237918004
- Waardenburg syndrome with limb anomalies237918004
- Telecanthus246803005
- Arnold-Chiari syndrome253184003
- Chiari malformation253184003
- Arnold Chiari type 1253185002
- Chiari malformation type I253185002
- Duplication of fibula253942007
- Short rib dysplasia254050009
- Short rib syndrome254050009
- TRPS I - Trichorhinophalangeal syndrome I254091006
- Trichorhinophalangeal dysplasia type I254091006
- Trichorhinophalangeal syndrome I254091006
- Alligator skin254156001
- Congenital ichthyosiform erythroderma254156001
- Amelia of lower limb265798000
- Congenital complete absence of lower limb265798000
- Acrocephalosyndactyly268262006
- Ichthyosiform dermatosis268282005
- Ichthyosiform erythroderma268282005
- Bent bone dysplasia group278832007
- Trichorhinophalangeal dysplasia type III389166003
- Congenital dysplasia of patella389276005
- Patella dysplasia389276005
- Port-wine stain in Rubinstein-Taybi syndrome403765001
- Acrocephalopolysyndactyly type 3403768004
- Acrocephalopolysyndactyly type III403768004
- Sakati-Nyhan syndrome403768004
- Disorder characterised by multiple exostoses410063006
- Disorder characterized by multiple exostoses410063006
- RAPADILINO - radial ray malformations, patella and palate abnormalities, diarrhea and dislocated joints, limb abnormalities and little size, slender nose and normal intelligence702413000
- RAPADILINO - radial ray malformations, patella and palate abnormalities, diarrhoea and dislocated joints, limb abnormalities and little size, slender nose and normal intelligence702413000
- RAPADILINO syndrome702413000
- Hand-foot-genital syndrome702425002
- Hand-foot-uterus syndrome702425002
- Jackson-Weiss syndrome709105005
- Mirror polydactyly, vertebral segmentation and limb defect syndrome715523005
- LBWC (limb body wall complex) syndrome716106000
- Limb body wall complex716106000
- Spondylocamptodactyly syndrome716231009
- Tetra-amelia with multiple malformation syndrome716249009
- Tetraamelia with multiple malformation syndrome716249009
- Zimmer phocomelia716249009
- X-linked intellectual disability Stevenson type718909001
- WT limb blood syndrome719019000
- Cousin syndrome719299009
- Familial pelvis-scapular dysplasia719299009
- Pelviscapular dysplasia719299009
- Pelviscapular dysplasia syndrome719299009
- Tel Hashomer camptodactyly syndrome719946008
- Acro-pectoral syndrome720412009
- Acropectoral syndrome720412009
- Syndactyly with preaxial polydactyly and sternal deformity syndrome720412009
- Acro-renal-ocular syndrome720415006
- Acrorenoocular syndrome720415006
- Acrorenal syndrome720458005
- ADULT (acro-dermato-ungual-lacrimal-tooth) syndrome720464003
- Acro-dermato-ungual-lacrimal-tooth syndrome720464003
- Campomelia Cumming type720599002
- Cumming syndrome720599002
- Camptodactyly with fibrous tissue hyperplasia and skeletal dysplasia syndrome720600004
- Goodman camptodactyly720600004
- CATSHL (camptodactyly, tall stature, scoliosis, hearing loss) syndrome720601000
- Camptodactyly and tall stature with scoliosis and hearing loss syndrome720601000
- Cooks syndrome720747002
- Berant syndrome720815000
- Capra DeMarco syndrome720815000
- Craniosynostosis, hydrocephalus, Arnold Chiari I malformation, radioulnar synostosis720815000
- Familial scaphocephaly with radioulnar synostosis syndrome720815000
- Agenesis of corpus callosum with polysyndactyly syndrome720819006
- Curry Jones syndrome720819006
- Fibular dimelia diplopodia syndrome720953006
- Leg duplication mirror foot syndrome720953006
- Fuhrmann Rieger de Sousa syndrome721296004
- Fuhrmann syndrome721296004
- Acro-fronto-facio-nasal dysostosis type 2721835008
- Acrofrontofacionasal dysostosis type 2721835008
- Hypertelorism, hypospadias, polysyndactyly syndrome721835008
- Naguib Richieri Costa syndrome721835008
- Congenital microgastria with limb reduction defect syndrome721880009
- IVIC (Instituto Venezolano de Investigaciones Cientificas) syndrome722019000
- IVIC syndrome722019000
- Oculo-oto-radial syndrome722019000
- Oculootoradial syndrome722019000
- Karsch Neugebauer syndrome722032005
- Ballard syndrome722298001
- Brachydactyly types B and E combined722298001
- Pitt Williams brachydactyly722298001
- Catel Manzke syndrome722383001
- Micrognathia digital syndrome722383001
- Palatodigital syndrome Catel-Manzke type722383001
- Guttmacher syndrome722452004
- Preaxial deficiency, postaxial polydactyly, hypospadias syndrome722452004
- EE - epileptic encephalopathy723125008
- Epileptic encephalopathy723125008
- PHAVER (pterygia, heart anomaly, autosomal recessive inheritance, vertebral defect, ear anomaly, radial defect) syndrome723453002
- PHAVER syndrome723453002
- Powell Chandra Saal syndrome723453002
- Pterygia, heart anomaly, autosomal recessive inheritance, vertebral defect, ear anomaly, radial defect syndrome723453002
- STAR (syndactyly, telecanthus, anogenital, renal malformation) syndrome723581006
- STAR syndrome723581006
- Syndactyly, telecanthus, anogenital and renal malformation syndrome723581006
- Sirenomelia sequence723973002
- Sirenomelus723973002
- Cryptomicrotia brachydactyly syndrome725096002
- Cryptomicrotia, brachydactyly, excess fingertip arch syndrome725096002
- Tonoki Ohura Niikawa syndrome725096002
- Severe intellectual disability, hypoplasia of thumb and hallux syndrome725140007
- Temple Baraitser syndrome725140007
- Deletion of part of chromosome 4726371001
- Dystopia canthorum726407000
- Caudal appendage deafness syndrome726621009
- Lynch Lee Murday syndrome726621009
- Banki syndrome733093004
- Brachydactyly long thumb type733454004
- Long thumb brachydactyly syndrome733454004
- Congenital mixed conductive and sensorineural hearing loss737377004
- Amniotic band syndrome765206003
- Congenital constriction band765206003
- Constriction ring syndrome765206003
- Deformity due to amniotic band765206003
- Temtamy preaxial brachydactyly syndrome777998000
- Rivera Perez Salas syndrome783003009
- Thoracolimb dysplasia Rivera type783003009
- Thoracomelic dysplasia783003009
- Antecubital pterygium syndrome784351000
- Trichorhinophalangeal syndrome type 1 and 3818959006
- Trichorhinophalangeal syndrome type I and III818959006
- ACFS - acrocardiofacial syndrome890221004
- Acro-cardio-facial syndrome890221004
- Acrocardiofacial syndrome890221004
- CCGE - cleft palate, cardiac defect, genital anomalies, ectrodactyly syndrome890221004
- Cleft palate, cardiac defect, genital anomalies, and ectrodactyly890221004
- Bilateral amelia of lower limbs890222006
- Congenital complete absence of bilateral lower limbs890222006
- Bilateral amelia of upper limbs890223001
- Congenital complete absence of bilateral upper limbs890223001
- Congenital anomaly of patella890399008
- Pfeiffer syndrome type 11003877009
- Proximal deletion of long arm of chromosome 41003900006
- Pfeiffer syndrome type 21003916008
- Pfeiffer syndrome type 31003918009
- Conductive hearing loss of right ear1010236009
- Conductive hearing loss of left ear1010238005
- Fetal sirenomelia1144273005
- Foetal sirenomelia1144273005
- Sireniform fetus1144273005
- Sireniform foetus1144273005
- Congenital hypoplasia of bone of pelvis1145432000
- Aplasia of bone of forearm1145452004
- Aplasia of bone of radius and/or ulna1145452004
- Aplasia of radius1145466009
- Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome1197591008
- Amelia of right lower extremity1201776003
- Amelia of right lower limb1201776003
- Congenital complete absence of right lower limb1201776003
- Amelia of left lower extremity1201777007
- Amelia of left lower limb1201777007
- Congenital complete absence of left lower limb1201777007
- PDE4D haploinsufficiency syndrome1236843008
- Phosphodiesterase 4D haploinsufficiency syndrome1236843008
- 4q25 proximal deletion syndrome1251452003
- Proximal monosomy 4q251251452003
- Amelia of left upper limb1258935001
- Congenital complete absence of left upper limb1258935001
- Amelia of right upper limb1258936000
- Congenital complete absence of right upper limb1258936000
- Mesomelic dysplasia of lower limb1263481007
- Congenital radioulnar synostosis1268409009
- EN1-related dorsoventral syndrome1340173008
- ENDOVE syndrome1340173008
- ENDOVES - EN1-related dorsoventral syndrome1340173008
- Mesomelic dysplasia, digital anomalies, intellectual disability syndrome1363286000
- Mixed conductive and sensorineural hearing loss of left ear18701000119107
- Mixed conductive and sensorineural hearing loss of right ear18711000119105
UMLS
- ANGIOOSTEOHYPERTROPHY SYNDROMEC0022739
- Angio Osteohypertrophy SyndromeC0022739
- Angio-Osteohypertrophy SyndromeC0022739
- Angio-Osteohypertrophy SyndromesC0022739
- Angio-osteohypertrophic syndromeC0022739
- Angio-osteohypertrophic syndrome (disorder)C0022739
- Angio-osteohypertrophy syndromeC0022739
- Angioosteohypertrophic syndromeC0022739
- Angioosteohypertrophy SyndromeC0022739
- Angioosteohypertrophy SyndromesC0022739
- Angiopathies, Congenital DysplasticC0022739
- Angiopathy, Congenital DysplasticC0022739
- Congenital Dysplastic AngiopathiesC0022739
- Congenital Dysplastic AngiopathyC0022739
- Congenital dysplastic angiopathyC0022739
- Disease, Klippel-TrenaunayC0022739
- Dysplastic Angiopathies, CongenitalC0022739
- Dysplastic Angiopathy, CongenitalC0022739
- KLIPPEL TRENAUNAY DISC0022739
- KLIPPEL-TRENAUNAY SYNDROMEC0022739
- KLIPPEL-TRENAUNAY-WEBER SYNDROMEC0022739
- KTSC0022739
- KTW SYNDROMEC0022739
- KTW SyndromeC0022739
- KTW SyndromesC0022739
- Klippel Trenaunay DiseaseC0022739
- Klippel Trenaunay SyndromeC0022739
- Klippel Trenaunay Weber SyndromeC0022739
- Klippel Trénaunay Weber SyndromeC0022739
- Klippel-Trenaunay DiseaseC0022739
- Klippel-Trenaunay SyndromeC0022739
- Klippel-Trenaunay SyndromesC0022739
- Klippel-Trenaunay-Weber SyndromeC0022739
- Klippel-Trenaunay-Weber syndromeC0022739
- Klippel-Trénaunay-Weber SyndromeC0022739
- Parkes-Weber syndromeC0022739
- Syndrome, Angio-OsteohypertrophyC0022739
- Syndrome, AngioosteohypertrophyC0022739
- Syndrome, KTWC0022739
- Syndrome, Klippel TrenaunayC0022739
- Syndrome, Klippel-TrenaunayC0022739
- Syndrome, Klippel-Trenaunay-WeberC0022739
- Syndrome, Klippel-Trénaunay-WeberC0022739
- Syndromes, Angio-OsteohypertrophyC0022739
- Syndromes, AngioosteohypertrophyC0022739
- Syndromes, KTWC0022739
- Syndromes, Klippel-TrenaunayC0022739
- klippel syndrome trenaunay weberC0022739
- klippel trenaunay weber syndromeC0022739
- klippel weber trenaunay syndromeC0022739
- klippel-trenaunay syndromeC0022739
- klippel-trenaunay-weber syndromeC0022739
- parkes weber syndromeC0022739
- syndrome klippel-trenaunay-weberC0022739
- syndrome webersC0022739
- weber syndromeC0022739
- webers syndromeC0022739
- ATRIODIGITAL DYSPLASIAC0265264
- Atrio-Digital SyndromeC0265264
- Atrio-digital syndromeC0265264
- Atriodigital dysplasiaC0265264
- Atriodigital dysplasia type 1C0265264
- Cardiac-Limb SyndromeC0265264
- Cardiac-limb syndromeC0265264
- HEART-HAND SYNDROMEC0265264
- HOLT-ORAM SYNDROMEC0265264
- HOSC0265264
- HOS1C0265264
- Heart-Hand Syndrome, Type 1C0265264
- Heart-hand syndromeC0265264
- Heart-hand syndrome type 1C0265264
- Heart-hand syndrome, type 1C0265264
- Holt Oram syndromeC0265264
- Holt-Oram SyndromeC0265264
- Holt-Oram syndromeC0265264
- Holt-Oram syndrome (disorder)C0265264
- Ventriculo-Radial SyndromeC0265264
- Ventriculo-radial syndromeC0265264
- holt oram syndromeC0265264
- holt-oram syndromeC0265264
- Absent radii and thrombocytopeniaC0175703
- CHROMOSOME 1q21.1 DELETION SYNDROME, 200-KBC0175703
- Chromosome 1q21.1 Deletion Syndrome, 200-KbC0175703
- Chromosome 1q21.1 deletion syndrome, 200-KBC0175703
- Radial Aplasia-Amegakaryocytic ThrombocytopeniaC0175703
- Radial Aplasia-Thrombocytopenia SyndromeC0175703
- Radial aplasia-amegakaryocytic thrombocytopeniaC0175703
- Radial aplasia-thrombocytopenia syndromeC0175703
- Radial aplasia-thrombocytopenia syndrome (disorder)C0175703
- TARC0175703
- TAR - Thrombocytopenia with absent radius syndromeC0175703
- TAR SYNDROMEC0175703
- TAR SyndromeC0175703
- TAR syndromeC0175703
- THROMBOCYTOPENIA-ABSENT RADIUS SYNDROMEC0175703
- Thrombocytopenia Absent RadiiC0175703
- Thrombocytopenia absent radiiC0175703
- Thrombocytopenia absent radius syndromeC0175703
- Thrombocytopenia with absent radius [TAR] syndromeC0175703
- Thrombocytopenia with absent radius syndromeC0175703
- Thrombocytopenia-Absent Radius SyndromeC0175703
- Thrombocytopenia-absent radii syndromeC0175703
- Thrombocytopenia-absent radius syndromeC0175703
- syndrome tarC0175703
- syndrome tarsC0175703
- tar syndromeC0175703
- BROAD THUMB-HALLUX SYNDROMEC0035934
- BROAD THUMBS AND GREAT TOES, CHARACTERISTIC FACIES, AND MENTAL RETARDATIONC0035934
- Broad Thumb Hallux SyndromeC0035934
- Broad Thumb-Hallux SyndromeC0035934
- Broad Thumb-Hallux SyndromesC0035934
- Broad Thumbs and Great Toes, Characteristic Facies, and Mental RetardationC0035934
- Broad thumb-hallux syndromeC0035934
- RSTSC0035934
- RTSC0035934
- RUBINSTEIN SYNDROMEC0035934
- Rubinstein SyndromeC0035934
- Rubinstein Taybi SyndromeC0035934
- Rubinstein-Taybi SyndromeC0035934
- Rubinstein-Taybi syndromeC0035934
- Rubinstein-Taybi syndrome (disorder)C0035934
- Syndrome, Broad Thumb-HalluxC0035934
- Syndrome, RubinsteinC0035934
- Syndrome, Rubinstein-TaybiC0035934
- Syndromes, Broad Thumb-HalluxC0035934
- rubenstein taybi syndromeC0035934
- rubenstein-taybi syndromeC0035934
- rubinstein syndromeC0035934
- rubinstein taybi syndromeC0035934
- rubinstein taybis syndromeC0035934
- rubinstein-taybi syndromeC0035934
- syndrome rubinstein taybiC0035934
- Congenital malformation syndromes predom involving limbsC0431766
- Congenital malformation syndromes predominantly involving limbsC0431766
- Disease, FongC0027341
- FONG DISEASEC0027341
- Fong DiseaseC0027341
- Fong diseaseC0027341
- Hereditary Onycho-OsteodysplasiaC0027341
- Hereditary Osteo-OnychodysplasiaC0027341
- Hereditary Osteo-OnychodysplasiasC0027341
- Hereditary onycho-osteodysplasiaC0027341
- Hereditary osteo-onychodysplasiaC0027341
- NAIL-PATELLA SYNDROMEC0027341
- NPSC0027341
- NPS1C0027341
- Nail Patella SyndromeC0027341
- Nail patella syndromeC0027341
- Nail-Patella SyndromeC0027341
- Nail-patella syndromeC0027341
- Nail-patella syndrome (disorder)C0027341
- ONYCHOOSTEODYSPLASIAC0027341
- OnychoosteodysplasiaC0027341
- Osteo Onychodysplasia, HereditaryC0027341
- Osteo-Onychodysplasia, HereditaryC0027341
- Osteo-Onychodysplasias, HereditaryC0027341
- Osterreicher SyndromeC0027341
- Osterreicher syndromeC0027341
- Pelvic Horn SyndromeC0027341
- Pelvic horn syndromeC0027341
- Syndrome, Nail-PatellaC0027341
- Syndrome, OsterreicherC0027341
- Syndrome, Pelvic HornC0027341
- Syndrome, Turner-KieserC0027341
- TURNER-KIESER SYNDROMEC0027341
- Turner Kieser SyndromeC0027341
- Turner Kieser syndromeC0027341
- Turner-Kieser SyndromeC0027341
- Turner-Kieser syndromeC0027341
- fong syndromeC0027341
- nail patella syndromeC0027341
- nail-patella syndromeC0027341
- turner kieser syndromeC0027341
- turner-kieser syndromeC0027341
- Sirenomelia syndromeC1406717
- VATER anomaladC0220708
- VATER associationC0220708
- VATER syndromeC0220708
- Vertebral anomalies/dysgenesis, anal atresia, tracheo-esophageal fistula, esophageal atresia, renal anomalies, radial dysplasia (VATER) associationC0220708
- Vertebral anomalies/dysgenesis, anal atresia, tracheo-esophageal fistula, esophageal atresia, renal anomalies, radial dysplasia associationC0220708
- Vertebral anomalies/dysgenesis, anal atresia, tracheo-esophageal fistula, esophageal atresia, renal anomalies, radial dysplasia association (disorder)C0220708
- Vertebral anomalies/dysgenesis, anal atresia, tracheo-oesophageal fistula, oesophageal atresia, renal anomalies, radial dysplasia (VATER) associationC0220708
- Vertebral anomalies/dysgenesis, anal atresia, tracheo-oesophageal fistula, oesophageal atresia, renal anomalies, radial dysplasia associationC0220708
- Vertebral defects, Anal atresia, Tracheoesophageal fistula with Esophageal atresia, and Radial dysplasiaC0220708
- association disorder vatersC0220708
- association vaterC0220708
- association vatersC0220708
- syndrome vaterC0220708
- syndrome vatersC0220708
- vater associationC0220708
- vater syndromeC0220708
Frequently Asked Questions
What is ICD-10 code Q87.2?
ICD-10-CM code Q87.2 represents "Congenital malformation syndromes predominantly involving limbs". It is a billable/specific code that can be used on a claim.
Is Q87.2 a billable code?
Yes, Q87.2 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q87.2 in?
Q87.2 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
Are additional codes required with Q87.2?
Yes, when using Q87.2 you should also code: code(s) to identify all associated manifestations.
What SNOMED CT codes does Q87.2 map to?
Q87.2 maps to 142 SNOMED CT concepts: 37506004, 1251452003, 890221004, 720464003, 71988008, and 137 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q87.2?
Q87.2 is linked to 8 UMLS Concept Unique Identifiers: C0022739, C0265264, C0175703, C0035934, C0431766, and 3 more. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.