AutoICD API

Q87.2

Billable

Congenital malformation syndromes predom involving limbs

Congenital malformation syndromes predominantly involving limbs

Status

Billable / Specific

Parent Code

Q87

ICD-11 Mapping

1 equivalent

Coding 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

Use Additional Code

Additional codes that should follow this code

  • code(s) to identify all associated manifestations
Related Codes(6)
Q87.0

Congen malform syndromes predom affecting facial appearance

BillableQ87.1

Congenital malform syndromes predom assoc w short stature

Q87.3

Congenital malformation syndromes involving early overgrowth

BillableQ87.4

Marfan syndrome

Q87.5

Oth congenital malformation syndromes w oth skeletal changes

BillableQ87.8

Oth congenital malformation syndromes, NEC

ICD-11 Equivalents(1)

ICD-11 Equivalents

View full mapping

Corresponding ICD-11 codes from the WHO crosswalk mapping

LD2ZMultiple developmental anomalies or syndromes, unspecifiedequivalentPrimary
Also Known As / Clinical Terms(937)

SNOMED CT

UMLS

Clinical Terms

  • HOLT-ORAM SYNDROME
  • Acrorenal syndrome
  • Conductive hearing loss of right ear
  • Pfeiffer syndrome
  • Escobar syndrome
  • CATSHL (camptodactyly, tall stature, scoliosis, hearing loss) syndrome
  • Naguib Richieri Costa syndrome
  • Brachymesophalangia
  • Radial aplasia-thrombocytopenia syndrome (disorder)
  • vater syndrome
  • Klein-Waardenberg syndrome
  • Angiopathy, Congenital Dysplastic
  • Amelia of right lower extremity
  • Hypoplastic anaemia
  • rubinstein taybis syndrome
  • Osteo-Onychodysplasia, Hereditary
  • Amelia of right upper limb
  • Aproctia
  • Chromosome 4q deletion syndrome
  • CHILD syndrome
  • Osteo Onychodysplasia, Hereditary
  • TRPS I - Trichorhinophalangeal syndrome I
  • Angioosteohypertrophy Syndrome
  • Scaphocephaly
  • Chiari malformation type I
  • Thrombocytopenia with absent radius syndrome
  • RUBINSTEIN SYNDROME
  • RAPADILINO - radial ray malformations, patella and palate abnormalities, diarrhea and dislocated joints, limb abnormalities and little size, slender nose and normal intelligence
  • Chromosome 1q21.1 Deletion Syndrome, 200-Kb
  • Atriodigital dysplasia type 1
  • Hereditary osteo-onychodysplasia
  • Disease, Klippel-Trenaunay
  • Congenital constriction band
  • syndrome vater
  • Nager acrofacial dysostosis syndrome
  • Conductive hearing loss, bilateral
  • Nail-patella syndrome
  • Bilateral amelia of lower limbs
  • STAR syndrome
  • HOS1
  • Syndactyly with preaxial polydactyly and sternal deformity syndrome
  • Syndrome, Rubinstein
  • Onychoosteodysplasia
  • Pfeiffer syndrome type 2
  • Disorder characterized by multiple exostoses
  • Antecubital pterygium syndrome
  • Aplasia of radius
  • Congenital hypoplastic anaemia Blackfan-Diamond type
  • HOS
  • Interparietal craniosynostosis
  • Osteo-Onychodysplasias, Hereditary
  • Congenital complete absence of bilateral lower limbs
  • Pfeiffer syndrome type 3
  • Thrombocytopenia-absent radii syndrome
  • Foetal sirenomelia
  • Trichorhinophalangeal dysplasia type III
  • Syndrome, Osterreicher
  • Transverse deficiency of arm, shoulder level
  • syndrome tar
  • Camptodactyly and tall stature with scoliosis and hearing loss syndrome
  • Acro-fronto-facio-nasal dysostosis type 2
  • Broad Thumbs and Great Toes, Characteristic Facies, and Mental Retardation
  • Congenital short femur
  • Vertebral anomalies/dysgenesis, anal atresia, tracheo-esophageal fistula, esophageal atresia, renal anomalies, radial dysplasia association (disorder)
  • Rubinstein Taybi Syndrome
  • Syndrome, Klippel-Trénaunay-Weber
  • Congenital complete absence of lower limb
  • Acropectoral syndrome
  • Heart-hand syndrome, type 1
  • Mirror polydactyly, vertebral segmentation and limb defect syndrome
  • Acro-dermato-ungual-lacrimal-tooth syndrome
  • Sakati-Nyhan syndrome
  • Waardenburg's syndrome
  • PDE4D haploinsufficiency syndrome
  • Congenital hypoplastic anemia
  • Trichorhinophalangeal syndrome type I and III
  • Mesomelic dysplasia of lower limb
  • Hand-foot-genital syndrome
  • Klippel-Trenaunay Syndromes
  • Cardiac-Limb Syndrome
  • Split foot
  • Temple Baraitser syndrome
  • Acro-renal-ocular syndrome
  • Sireniform fetus
  • Heart-hand syndrome type 1
  • Lobster-claw hand
  • Tel Hashomer camptodactyly syndrome
  • Caudal appendage deafness syndrome
  • KTW Syndromes
  • turner kieser syndrome
  • Acrocephalosyndactyly type V
  • Klippel-Trenaunay Syndrome
  • Parkes-Weber syndrome
  • PHAVER syndrome
  • nail patella syndrome
  • Short rib dysplasia
  • Mixed hearing loss
  • syndrome tars
  • Radial aplasia-amegakaryocytic thrombocytopenia
  • Mesomelic dysplasia - Nievergelt type
  • Short rib syndrome
  • Nager syndrome
  • Arnold Chiari type 1
  • Brachydactyly types B and E combined
  • Craniosynostosis, hydrocephalus, Arnold Chiari I malformation, radioulnar synostosis
  • Proximal deletion of long arm of chromosome 4
  • THROMBOCYTOPENIA-ABSENT RADIUS SYNDROME
  • Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome
  • Long thumb brachydactyly syndrome
  • Syndrome, KTW
  • Congenital complete absence of right lower limb
  • Severe intellectual disability, hypoplasia of thumb and hallux syndrome
  • Syndromes, Klippel-Trenaunay
  • Thoracolimb dysplasia Rivera type
  • Brachydactyly long thumb type
  • Congenital pure red cell anaemia
  • Hypoplastic anemia - familial
  • Angio-Osteohypertrophy Syndrome
  • Cumming syndrome
  • Congenital complete absence of upper limb
  • Lobster claw foot
  • Pfeiffer-type acrocephalosyndactyly
  • Vertebral anomalies/dysgenesis, anal atresia, tracheo-esophageal fistula, esophageal atresia, renal anomalies, radial dysplasia (VATER) association
  • Jackson-Weiss syndrome
  • Capra DeMarco syndrome
  • Syndactyly, telecanthus, anogenital and renal malformation syndrome
  • Vertebral defects, Anal atresia, Tracheoesophageal fistula with Esophageal atresia, and Radial dysplasia
  • Trichorhinophalangeal syndrome
  • Hereditary onycho-osteodysplasia
  • Syndrome, Pelvic Horn
  • Thrombocytopenia with absent radius [TAR] syndrome
  • Acrocephalopolysyndactyly
  • Amelia of left upper limb
  • Karsch Neugebauer syndrome
  • TAR - Thrombocytopenia with absent radius syndrome
  • Temtamy preaxial brachydactyly syndrome
  • syndrome rubinstein taybi
  • Phosphodiesterase 4D haploinsufficiency syndrome
  • fong syndrome
  • CHILD (congenital hemidysplasia, ichthyosiform erythroderma, limb defects) syndrome
  • Micrognathia digital syndrome
  • Cryptomicrotia, brachydactyly, excess fingertip arch syndrome
  • Lacrimo-auriculo-dento-digital syndrome
  • Angio-osteohypertrophic syndrome (disorder)
  • Chronic constitutional pure red cell anemia
  • Osterreicher Syndrome
  • Sirenomelia syndrome
  • Brachydactyly of toes
  • 4q25 proximal deletion syndrome
  • Acro-cardio-facial syndrome
  • STAR (syndactyly, telecanthus, anogenital, renal malformation) syndrome
  • Congenital hemidysplasia with ichthyosiform erythroderma and limb defects syndrome
  • Congenital hypoplastic anaemia
  • Hereditary Osteo-Onychodysplasias
  • Broad Thumb Hallux Syndrome
  • LBWC (limb body wall complex) syndrome
  • Syndrome, Angio-Osteohypertrophy
  • syndrome klippel-trenaunay-weber
  • Broad Thumb-Hallux Syndromes
  • Aase Smith II syndrome
  • Waardenburg syndrome with limb anomalies
  • rubinstein-taybi syndrome
  • PHAVER (pterygia, heart anomaly, autosomal recessive inheritance, vertebral defect, ear anomaly, radial defect) syndrome
  • ACFS - acrocardiofacial syndrome
  • Aplasia of bone of radius and/or ulna
  • Lynch Lee Murday syndrome
  • Congenital atresia of anus
  • Rivera Perez Salas syndrome
  • Pelvic horn syndrome
  • Mixed conductive and sensorineural hearing loss of right ear
  • Nievergelt syndrome
  • Amelia of upper limb
  • Constitutional aplastic anemia
  • Ruvalcaba syndrome
  • VATER anomalad
  • Angio Osteohypertrophy Syndrome
  • Telecanthus
  • Congenital microgastria with limb reduction defect syndrome
  • Mixed conductive and sensorineural hearing loss, bilateral
  • Port-wine stain in Rubinstein-Taybi syndrome
  • Holt Oram syndrome
  • Epileptic encephalopathy
  • Congenital Dysplastic Angiopathy
  • Ventriculo-radial syndrome
  • Congenital complete absence of left upper limb
  • Aase syndrome
  • ENDOVES - EN1-related dorsoventral syndrome
  • Sensorineural hearing loss of both ears
  • Proximal monosomy 4q25
  • Tetra-amelia with multiple malformation syndrome
  • IVIC (Instituto Venezolano de Investigaciones Cientificas) syndrome
  • Congenital cleft hand
  • Pterygia, heart anomaly, autosomal recessive inheritance, vertebral defect, ear anomaly, radial defect syndrome
  • FONG DISEASE
  • KLIPPEL TRENAUNAY DIS
  • Ichthyosiform dermatosis
  • syndrome webers
  • TRPS II - Trichorhinophalangeal syndrome II
  • Congenital imperforate anus
  • Klippel-Trenaunay-Weber Syndrome
  • Cryptomicrotia brachydactyly syndrome
  • Mesomelic dysplasia, digital anomalies, intellectual disability syndrome
  • Familial hypoplastic anemia
  • Arnold-Chiari syndrome
  • Deformity due to amniotic band
  • Radial Aplasia-Thrombocytopenia Syndrome
  • Syndromes, Angioosteohypertrophy
  • Fibular dimelia diplopodia syndrome
  • Townes Brocks syndrome
  • Congenital complete absence of left lower limb
  • Trichorhinophalangeal syndrome II
  • NPS1
  • Congenital hypoplasia of bone of pelvis
  • Chronic constitutional pure red cell anaemia
  • klippel trenaunay weber syndrome
  • Sirenomelia sequence
  • KTW Syndrome
  • Thoracomelic dysplasia
  • KTS
  • Congenital small stomach
  • Grebe dysplasia
  • webers syndrome
  • Mixed type deafness
  • RSTS
  • Acrofrontofacionasal dysostosis type 2
  • Vertebral anomalies/dysgenesis, anal atresia, tracheo-oesophageal fistula, oesophageal atresia, renal anomalies, radial dysplasia (VATER) association
  • Saethre-Chotzen syndrome
  • Atrio-Digital Syndrome
  • Oculootoradial syndrome
  • Sagittal synostosis
  • Thrombocytopenia Absent Radii
  • Camptodactyly with fibrous tissue hyperplasia and skeletal dysplasia syndrome
  • RTS
  • Amegakaryocytic thrombocytopenia
  • Angioosteohypertrophic syndrome
  • Broad Thumb-Hallux Syndrome
  • Levy-Hollister syndrome
  • Rubinstein-Taybi syndrome (disorder)
  • Amelia of left lower extremity
  • Duplication of fibula
  • X-linked intellectual disability Stevenson type
  • IVIC syndrome
  • Atresia ani
  • Multiple malformation syndrome, small stature, without skeletal dysplasia
  • Acrocephalopolysyndactyly type 3
  • Disease, Fong
  • Femoral facial syndrome
  • Mixed conductive AND sensorineural hearing loss
  • Congenital erythroid hypoplasia
  • ADULT (acro-dermato-ungual-lacrimal-tooth) syndrome
  • Multiple malformation syndrome with facial-limb defects as major feature
  • Thrombocytopenia absent radius syndrome
  • parkes weber syndrome
  • MHL - Mixed hearing loss
  • Congenital ichthyosiform erythroderma
  • Congenital gastric hypoplasia
  • Amelia of lower limb
  • Constriction ring syndrome
  • Syndromes, KTW
  • Berant syndrome
  • tar syndrome
  • EN1-related dorsoventral syndrome
  • VATER association
  • Oculo-oto-radial syndrome
  • 4q partial monosomy syndrome
  • Congenital anomaly of patella
  • Pelviscapular dysplasia
  • Townes syndrome
  • Zimmer phocomelia
  • Chiari malformation
  • Acrocephalosyndactyly type 5
  • Agenesis of corpus callosum with polysyndactyly syndrome
  • Syndrome, Broad Thumb-Hallux
  • Cleft palate, cardiac defect, genital anomalies, and ectrodactyly
  • association vaters
  • Acro-pectoral syndrome
  • Type 2 aplasia cutis
  • Congenital absence of radius
  • Acrocardiofacial syndrome
  • Cleft foot
  • Hand-foot-uterus syndrome
  • Congenital red cell aplasia
  • Fuhrmann Rieger de Sousa syndrome
  • turner-kieser syndrome
  • Patella dysplasia
  • HEART-HAND SYNDROME
  • Amniotic band syndrome
  • Powell Chandra Saal syndrome
  • WT limb blood syndrome
  • syndrome vaters
  • Microgastria
  • Banki syndrome
  • Sensorineural hearing loss of bilateral ears
  • Hypertelorism, hypospadias, polysyndactyly syndrome
  • Dystopia canthorum
  • Syndrome, Klippel Trenaunay
  • Nievergelt-Erb syndrome
  • Congenital complete absence of right upper limb
  • Syndrome, Rubinstein-Taybi
  • Congenital absence of skin on scalp with limb-reduction anomaly
  • Ballard syndrome
  • Klippel Trénaunay Weber Syndrome
  • Guttmacher syndrome
  • Deletion of part of chromosome 4
  • Congenital microgastria
  • Acrorenoocular syndrome
  • Congenital pure red cell anemia
  • Bilateral amelia of upper limbs
  • Goodman camptodactyly
  • Klippel-Trenaunay Disease
  • Congenital abnormal shape of fibula
  • Congenital hypoplastic anemia Blackfan-Diamond type
  • Syndromes, Angio-Osteohypertrophy
  • Amelia of right lower limb
  • Multiple malformation syndrome with limb defect as major feature
  • Familial scaphocephaly with radioulnar synostosis syndrome
  • Congenital anomaly of caudal vertebra
  • Angioosteohypertrophy Syndromes
  • Congenital aplastic anaemia
  • Langer-Giedion syndrome
  • Blackfan-Diamond anemia
  • Alligator skin
  • Sirenomelus
  • association vater
  • TAR
  • klippel syndrome trenaunay weber
  • Hypoplastic anaemia - familial
  • Tetraamelia with multiple malformation syndrome
  • Pfeiffer syndrome type 1
  • Congenital misshapen fibula
  • EE - epileptic encephalopathy
  • weber syndrome
  • Blackfan-Diamond anaemia
  • Preaxial deficiency, postaxial polydactyly, hypospadias syndrome
  • Preaxial acrofacial dysostosis
  • Waardenburg syndrome
  • Mixed conductive and sensorineural hearing loss of left ear
  • Mixed conductive and sensorineural deafness
  • Acromesomelic dysplasia Grebe type
  • Angio-Osteohypertrophy Syndromes
  • Angiopathies, Congenital Dysplastic
  • Waardenburg syndrome type 3
  • Pelviscapular dysplasia syndrome
  • Mixed deafness
  • Palatodigital syndrome Catel-Manzke type
  • Absent radii and thrombocytopenia
  • Aplasia of bone of forearm
  • Amelia of left lower limb
  • Congenital Dysplastic Angiopathies
  • Klein-Waardenberg's syndrome
  • Catel Manzke syndrome
  • Klippel Trenaunay Disease
  • Acrocephalosyndactyly, type III
  • Congenital complete absence of bilateral upper limbs
  • Lobster claw hand
  • Hypoplastic anemia
  • ATRIODIGITAL DYSPLASIA
  • Sireniform foetus
  • Trichorhinophalangeal syndrome I
  • Congenital abnormal shape of tibia
  • Vertebral anomalies/dysgenesis, anal atresia, tracheo-esophageal fistula, esophageal atresia, renal anomalies, radial dysplasia association
  • Erythrogenesis imperfecta
  • Limb reduction-ichthyosis syndrome
  • Pitt Williams brachydactyly
  • Acrocephalopolysyndactyly type III
  • Spondylocamptodactyly syndrome
  • Congenital radioulnar synostosis
  • Grebe syndrome
  • Congenital dysplasia of patella
  • Tonoki Ohura Niikawa syndrome
  • association disorder vaters
  • Familial pelvis-scapular dysplasia
  • Klippel-Trénaunay-Weber Syndrome
  • Trichorhinophalangeal dysplasia type I
  • RAPADILINO syndrome
  • rubenstein-taybi syndrome
  • Fetal sirenomelia
  • Chronic constitutional pure red cell aplasia
  • Trichorhinophalangeal syndrome with exostosis
  • Syndromes, Broad Thumb-Hallux
  • Leg duplication mirror foot syndrome
  • Congenital misshapen tibia
  • Congenital hypoplasia of femur
  • ENDOVE syndrome
  • Congenital pure red cell aplasia
  • Cousin syndrome
  • Familial hypoplastic anaemia
  • Nail-patella syndrome (disorder)
  • Curry Jones syndrome
  • Acrocephalosyndactyly
  • Syndrome, Angioosteohypertrophy
  • Vertebral anomalies/dysgenesis, anal atresia, tracheo-oesophageal fistula, oesophageal atresia, renal anomalies, radial dysplasia association
  • Imperforate anus
  • rubenstein taybi syndrome
  • Duplication of lower limb bone
  • Sagittal craniosynostosis
  • Mietens syndrome
  • Syndrome, Klippel-Trenaunay-Weber
  • Angio-osteohypertrophic syndrome
  • CCGE - cleft palate, cardiac defect, genital anomalies, ectrodactyly syndrome
  • Campomelia Cumming type
  • Klippel Trenaunay Syndrome
  • Bilateral hearing loss
  • Fuhrmann syndrome
  • Trichorhinophalangeal syndrome type 1 and 3
  • Congenital mixed conductive and sensorineural hearing loss
  • Conductive hearing loss of left ear
  • Syndrome, Klippel-Trenaunay
  • Holt-Oram syndrome (disorder)
  • NPS
  • Dysplastic Angiopathies, Congenital
  • Nievergelt's syndrome
  • Syndrome, Nail-Patella
  • Constitutional aplastic anaemia
  • Syndrome, Turner-Kieser
  • Bent bone dysplasia group
  • Cooks syndrome
  • Anal atresia
  • Dysplastic Angiopathy, Congenital
  • klippel weber trenaunay syndrome
  • RAPADILINO - radial ray malformations, patella and palate abnormalities, diarrhoea and dislocated joints, limb abnormalities and little size, slender nose and normal intelligence
  • Waardenburg syndrome type III
  • Femoral hypoplasia - unusual facies syndrome
  • Limb body wall complex
  • Disorder characterised by multiple exostoses
  • Ichthyosiform erythroderma
  • Adams-Oliver syndrome
  • Congenital aplastic anemia
Frequently Asked Questions
What is the ICD-10 code for congenital malformation syndromes predom involving limbs?

The ICD-10-CM code for congenital malformation syndromes predom involving limbs is Q87.2. The full clinical description is "Congenital malformation syndromes predominantly involving limbs". Q87.2 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q87.2 mean?

ICD-10-CM code Q87.2 represents “Congenital malformation syndromes predominantly involving limbs”. It is classified under Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities and 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, also report: 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.

How does Q87.2 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like congenital malformation syndromes predom involving limbs affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of Q87.2?

Q87.2 maps to the ICD-11 code: LD2Z (Multiple developmental anomalies or syndromes, unspecified).

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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.