Q87.89
BillableOth congenital malformation syndromes, NEC
Other specified congenital malformation syndromes, not elsewhere classified
Status
Billable / Specific
Parent Code
Q87.8Coding Notes
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- Zellweger syndrome (E71.510)
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
- 11p partial monosomy syndrome4135001
- Bardet-Biedl syndrome5619004
- Biedl-Bardet syndrome5619004
- LMBB - Laurence-Moon-Bardet-Biedl syndrome5619004
- Laurence-Moon-Biedl syndrome5619004
- Diabetes mellitus associated with genetic syndrome5969009
- Genetic syndromes of diabetes mellitus5969009
- VACTEL syndrome6839008
- Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, limb defects (VACTEL) syndrome6839008
- Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, limb defects syndrome6839008
- Distal arthrogryposis type 78757006
- Dutch Kentucky syndrome8757006
- Hecht Beals syndrome8757006
- Hecht syndrome8757006
- Trismus pseudocamptodactyly syndrome8757006
- Multiple malformation syndrome with senile-like appearance12674005
- Ablepharia13401001
- Ablepharon13401001
- Ablepharon - absent eyelids13401001
- Open eye13401001
- Congenital aplastic anaemia28975000
- Congenital aplastic anemia28975000
- Constitutional aplastic anaemia28975000
- Constitutional aplastic anemia28975000
- Hypoplastic anaemia - familial28975000
- Hypoplastic anemia - familial28975000
- Curtius' syndrome I38215007
- Oculodentodigital dysplasia38215007
- Oculodentodigital syndrome38215007
- Juvenile periodontosis with hyperkeratosis40158001
- Papillon-Lefevre syndrome40158001
- Papillon-Lefèvre syndrome40158001
- Partial ablepharon45484000
- Waardenburg syndrome47434006
- Waardenburg's syndrome47434006
- FG syndrome49984004
- Cleft iris51485001
- Congenital coloboma of iris51485001
- Notched iris51485001
- Cohen syndrome56604005
- Pallister-Hall syndrome56677004
- Athetoid movement58593005
- Autosomal recessive cutis laxa type III59252009
- Cutis laxa-corneal clouding-oligophrenia syndrome59252009
- Progeroid syndrome of de Barsey59252009
- de Barsey syndrome59252009
- de Barsey-Moens-Dierckx syndrome59252009
- Cutis laxa, autosomal recessive59451000
- Alstrom syndrome63702009
- Congenital absence of cilia of eyelid63935007
- Congenital absence of eyelash63935007
- Popliteal pterygium syndrome66783006
- Allemann syndrome70943004
- Allemann's syndrome70943004
- Hereditary choroidal atrophy74469006
- Hereditary choroidal dystrophy74469006
- Cole-Engmann-Zinsser syndrome74911008
- Congenital dyskeratosis74911008
- DKC - Dyskeratosis congenita74911008
- Dyskeratosis congenita74911008
- Zinsser-Cole-Engman syndrome74911008
- Zinsser-Cole-Engmann syndrome74911008
- Choroideraemia75241009
- Choroideremia75241009
- Tapetochoroidal dystrophy75241009
- Atresia of external auditory canal75355004
- Congenital atresia of external auditory canal75355004
- MHL - Mixed hearing loss77507001
- Mixed conductive AND sensorineural hearing loss77507001
- Mixed conductive and sensorineural deafness77507001
- Mixed deafness77507001
- Mixed hearing loss77507001
- Mixed type deafness77507001
- 3-phosphoglycerate dehydrogenase deficiency neonatal form77817004
- NLS - Neu-Laxova syndrome77817004
- Neu-Laxova syndrome77817004
- Multiple system malformation syndrome82354003
- PDA - Patent ductus arteriosus83330001
- Patent arterial duct83330001
- Patent ductus Botalli83330001
- Patent ductus arteriosus83330001
- Cochlear hearing loss85571008
- Inner ear hearing loss85571008
- Sensory hearing loss85571008
- Dysmotile cilia syndrome86204009
- ICS - Immotile cilia syndrome86204009
- Immotile cilia syndrome86204009
- PCD - Primary ciliary dyskinesia86204009
- Polynesian bronchiectasis86204009
- Primary ciliary dyskinesia86204009
- Exaggeration of the deep reflexes86854008
- Hyperreflexia86854008
- Increased tendon reflexes86854008
- Benign neoplasm of heart92132009
- Benign tumor of heart92132009
- Benign tumour of heart92132009
- Pure gonadal dysgenesis 46,XY95218005
- Swyer syndrome95218005
- Pure gonadal dysgenesis95219002
- Fixed dilatation of pupil103271006
- Fixed dilated pupil103271006
- Fixed pupil up103271006
- Interparietal craniosynostosis109418001
- Sagittal craniosynostosis109418001
- Sagittal synostosis109418001
- Scaphocephaly109418001
- Alveolar bone loss109706009
- Multiple fibrofolliculomas110985001
- Multiple fibrofolliculomata110985001
- Delayed bone age123983008
- Retarded bone age123983008
- Severe combined immunodeficiency with low T- and B-cell numbers190997006
- Intestinal lymphangiectasia197260007
- Intestinal lymphangiectasis197260007
- Periodic paralysis198030008
- Biemond syndrome205828009
- Biemond's syndrome205828009
- Slow to talk229721007
- Speech delay229721007
- X-linked retinitis pigmentosa232054005
- Laurence-Moon syndrome232059000
- Primary ciliary dyskinesia due to transposition of ciliary microtubules233663004
- Immotile cilia syndrome due to defective radial spokes233664005
- Azoospermia, obstructive and chronic sinopulmonary infections233666007
- Barry-Perkins-Young syndrome233666007
- Sinusitis-infertility syndrome233666007
- Young syndrome233666007
- Young's syndrome233666007
- Rutland ciliary disorientation syndrome233667003
- Hennekam lymphangiectasia-lymphedema syndrome234146006
- Hennekam lymphangiectasia-lymphoedema syndrome234146006
- Hennekam syndrome234146006
- Lymphedema, lymphangiectasia, intellectual disability syndrome234146006
- Lymphoedema, lymphangiectasia, intellectual disability syndrome234146006
- Adrenal gland hyperfunction237744009
- Adrenal hyperfunction237744009
- Hyperadrenalism237744009
- Micronodular adrenal hyperplasia237779006
- Polyglandular hyperfunction237827002
- Fetal acidosis240306004
- Foetal acidosis240306004
- Marfanoid physique248298009
- Congenital anomaly of the eyebrow253206006
- Congenital malformation of the eyebrow253206006
- Absent eyebrow253208007
- PPS - Peripheral pulmonary stenosis253631001
- Peripheral pulmonary artery stenosis253631001
- Singleton-Merten syndrome254114000
- Oculodento-osseous dysplasia254137006
- Oculodento-osseous dysplasia - severe type254138001
- Oculodento-osseous dysplasia - mild type254139009
- Dermochondrocorneal dystrophy254150007
- Francois syndrome254150007
- Fibrofolliculoma254699007
- Malabsorption of glucose267426009
- HF - Hydrops fetalis276508000
- HF - Hydrops foetalis276508000
- Hydrops fetalis276508000
- Hydrops foetalis276508000
- Disorder of serine metabolism303097007
- 3-Phosphoglycerate dehydrogenase deficiency303098002
- Costello syndrome309776008
- Floating-Harbor syndrome312214005
- Congenital anomaly of lymphatic structure of trunk363031002
- Hereditary disorder of lymphatic system363190001
- Fetal metabolic disorder363204006
- Metabolic disorder of fetus363204006
- Bone age finding397651006
- Nicolaides-Baraitser syndrome401046009
- Arthrogryposis multiplex congenita, pulmonary hypoplasia syndrome401138005
- FADS - fetal akinesia deformation sequence401138005
- FADS - foetal akinesia deformation sequence401138005
- Fetal akinesia-hypokinesia sequence401138005
- Foetal akinesia-hypokinesia sequence401138005
- Pena-Shokeir syndrome type I401138005
- Developmental malformation of branchial arch402810002
- Aplasia cutis congenita secondary to malformation syndrome (Type 9)403553002
- Aplasia cutis in Johanson-Blizzard syndrome403763008
- PIBIDS syndrome, photosensitivity with IBIDS403781006
- Photosensitivity with ichthyosis, brittle hair, impaired intelligence, decreased fertility and short stature syndrome403781006
- Currarino triad413936007
- Andersen Tawil syndrome422348008
- Andersen cardiodysrhythmic periodic paralysis422348008
- Long QT syndrome 7422348008
- Generalised dystonia425492002
- Generalized dystonia425492002
- Myxoma of heart426191007
- Anterior corneal dystrophy430888006
- Dystrophy of anterior cornea430888006
- VACTERL syndrome431395004
- Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, renal anomalies, limb defects (VACTERL) syndrome431395004
- Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, renal anomalies, limb defects syndrome431395004
- Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-oesophageal fistula, renal anomalies, limb defects (VACTERL) syndrome431395004
- Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-oesophageal fistula, renal anomalies, limb defects syndrome431395004
- Oto-onycho-peroneal syndrome441944007
- Rhombencephalosynapsis442300000
- Nance-Horan syndrome445257004
- Loeys-Dietz syndrome446263001
- Congenital stenosis of pulmonary artery449125001
- Marden Walker syndrome449824004
- Fetal anaemia462166006
- Fetal anemia462166006
- Foetal anaemia462166006
- Heritable pulmonary arterial hypertension697897003
- PHACE syndrome698765007
- Pascual Castroviejo syndrome type 2698765007
- Posterior fossa brain malformation, haemangioma, arterial anomaly, cardiac defect and aortic coarctation, and eye abnormality syndrome698765007
- Posterior fossa brain malformation, hemangioma, arterial anomaly, cardiac defect and aortic coarctation, and eye abnormality syndrome698765007
- Long QT syndrome with syndactyly699256006
- Timothy syndrome classic type699256006
- Timothy syndrome type 1699256006
- Blepharophimosis-intellectual disability syndrome Maat-Kievit-Brunner type699297004
- Blepharophimosis-mental retardation syndrome, Maat-Kievit-Brunner type699297004
- Ohdo syndrome, Maat-Kievit-Brunner type699297004
- X-linked Ohdo syndrome699297004
- Blepharophimosis, intellectual disability syndrome, Say-Barber-Biesecker-Young-Simpson type699298009
- Blepharophimosis-intellectual deficit syndrome, Say-Barber/Biesecker/Young-Simpson type699298009
- Hypothyroidism, dysmorphism, postaxial polydactyly, intellectual disability syndrome699298009
- Ohdo syndrome, Say-Barber-Biesecker-Young-Simpson variant699298009
- Say-Barber-Biesecker-Young-Simpson syndrome699298009
- Say-Barber-Biesecker-Young-Simpson variant of Ohdo syndrome699298009
- Young-Simpson syndrome699298009
- Microphthalmia syndromic 2699300009
- Microphthalmia, cataract, radiculomegaly and septal heart defect699300009
- Oculo-facio-cardio-dental syndrome699300009
- Oculofaciocardiodental syndrome699300009
- Facial dysmorphism, intellectual deficit, short stature and hearing loss699316006
- Laryngotracheal stenosis, arthropathy, prognathism and short stature699316006
- Myhre syndrome699316006
- Laband-Zimmermann syndrome699447001
- Zimmermann-Laband syndrome699447001
- Golabi-Ito-Hall syndrome699669001
- Hamel cerebropalatocardiac syndrome699669001
- Porteous syndrome699669001
- Renpenning syndrome699669001
- Sutherland-Haan syndrome699669001
- X-linked intellectual deficit due to PQBP1 mutation699669001
- Oculodental syndrome699754008
- Rutherfurd syndrome699754008
- Eccrine tumors ectodermal dysplasia700062000
- Eccrine tumours ectodermal dysplasia700062000
- Keratosis palmoplantaris, cystic eyelids, hypodontia, hypotrichosis syndrome700062000
- Palmoplantar hyperkeratosis, cystic eyelids, hypodontia, hypotrichosis syndrome700062000
- Palmoplantar keratoderma, cystic eyelids, hypodontia, hypotrichosis syndrome700062000
- SSPS - Schöpf Schulz Passarge syndrome700062000
- Schöpf Schulz Passarge syndrome700062000
- Schöpf-Schulz-Passarge syndrome700062000
- Christianson syndrome702354007
- X-linked Angelman-like syndrome702354007
- X-linked intellectual developmental disorder Christianson type702354007
- Craniofacial deafness hand syndrome702362004
- Sommer Young Wee Frye syndrome702362004
- Ciliary neurotrophic factor receptor-related disorder702363009
- Cold-induced sweating syndrome702363009
- Sohar-Crisponi syndrome702363009
- Hydrometrocolpos, postaxial polydactyly, and congenital heart malformation702407009
- McKusick Kaufman syndrome702407009
- DICER1 syndrome702411003
- Pleuropulmonary blastoma familial tumor and dysplasia syndrome702411003
- Pleuropulmonary blastoma familial tumour and dysplasia syndrome702411003
- Pleuropulmonary blastoma family tumor susceptibility syndrome702411003
- Pleuropulmonary blastoma family tumour susceptibility syndrome702411003
- Mental retardation, x-linked, Snyder-Robinson type702416008
- Snyder-Robinson syndrome702416008
- Snyder-Robinson x-linked mental retardation syndrome702416008
- X-linked intellectual disability Snyder type702416008
- Diaphragmatic hernia-exomphalos-corpus callosum agenesis702418009
- Diaphragmatic hernia-exomphalos-hypertelorism syndrome702418009
- Donnai-Barrow syndrome702418009
- Faciooculoacousticorenal syndrome702418009
- Feingold syndrome702431004
- Microcephaly-mesobrachyphalangy-tracheoesophageal fistula syndrome702431004
- Microcephaly-oculo-digito-esophageal-duodenal syndrome702431004
- Microcephaly-oculo-digito-oesophageal-duodenal syndrome702431004
- Oculo-digito-esophagoduodenal syndrome702431004
- Oculo-digito-oesophagoduodenal syndrome702431004
- Ear, patella, short stature syndrome703508009
- Meier-Gorlin syndrome703508009
- Microtia, absent patellae, micrognathia syndrome703508009
- Autosomal dominant dyskeratosis congenita707273001
- Periodontitis due to Papillon-Lefevre syndrome709472003
- Periodontitis due to Papillon-Lefèvre syndrome709472003
- Bowen Hutterite syndrome711153001
- Bowen-Conradi Hutterite syndrome711153001
- Bowen-Conradi syndrome711153001
- Hutterite syndrome711153001
- Biemond syndrome type 2717887003
- Autosomal dominant popliteal pterygium syndrome718222000
- Facio-genito-popliteal syndrome718222000
- Popliteal web syndrome718222000
- Fried syndrome718848000
- X-linked intellectual disability Pai type719011002
- Armfield syndrome719017003
- X-linked intellectual disability Armfield type719017003
- BSG syndrome719097002
- Branchio-skeleto-genital syndrome719097002
- Branchioskeletogenital syndrome719097002
- Primary ciliary dyskinesia and retinitis pigmentosa syndrome719282008
- Dionisi Vici Sabetta Gambarara syndrome719824001
- Vici syndrome719824001
- Haim Munk syndrome719973009
- Keratosis palmoplantaris with periodontopathia and onychogryposis syndrome719973009
- Bohring Opitz syndrome720565000
- Bohring syndrome720565000
- C-like syndrome720565000
- Opitz trigonocephaly-like syndrome720565000
- Bosley Salih Alorainy syndrome720567008
- Braddock syndrome720575002
- VATER-like syndrome with pulmonary hypertension, abnormal ear and growth deficiency720575002
- Cardiocranial syndrome Pfeiffer type720606005
- Craniosynostosis with congenital heart disease and intellectual disability syndrome720606005
- Pfeiffer Singer Zschiesche syndrome720606005
- Sagittal craniostenosis with congenital heart disease, mental deficiency and mandibular ankylosis720606005
- Aural atresia with multiple congenital anomalies and intellectual disability syndrome720748007
- Cooper Jabs syndrome720748007
- 3MC syndrome720756005
- Craniofacial ulnar renal syndrome720756005
- Cernunnos-XLF deficiency720853005
- NHEJ1 (non-homologous end joining factor) syndrome720853005
- Severe combined immunodeficiency due to Cernunnos protein deficiency720853005
- Severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionising radiation syndrome720853005
- Severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome720853005
- Siegler Brewer Carey syndrome721076000
- Developmental malformation, deafness, dystonia syndrome721092005
- Alopecia, anosmia, deafness, hypogonadism syndrome721584005
- Johnson McMillin syndrome721584005
- Johnson neuroectodermal syndrome721584005
- Juberg Hayward syndrome721874001
- Orocraniodigital syndrome721874001
- Lowry MacLean syndrome721974000
- Intellectual disability, balding, patella luxation, acromicria syndrome722002002
- Scholte Begeer-van Essen syndrome722002002
- Scholte syndrome722002002
- Cecatto de Lima Pinheiro syndrome722062004
- Oculotrichodysplasia722062004
- Athyroidal hypothyroidism with spiky hair and cleft palate syndrome722375007
- Bamforth Lazarus syndrome722375007
- Hypothyroidism and cleft palate syndrome722375007
- Autosomal recessive popliteal pterygium syndrome722376008
- Bartsocas Papas syndrome722376008
- Lethal popliteal pterygium syndrome722376008
- Baraitser Brett Piesowicz syndrome722390006
- Bilateral band-like calcification with polymicrogyria722390006
- Congenital intrauterine infection-like syndrome722390006
- Microcephaly, intracranial calcification, intellectual disability syndrome722390006
- Pseudo-TORCH syndrome722390006
- Cerebellotrigeminal dermal dysplasia syndrome722451006
- Gomez Lopez Hernandez syndrome722451006
- Anophthalmia with pulmonary hypoplasia syndrome722458000
- Matthew Wood syndrome722458000
- Syndromic microphthalmia type 9722458000
- Meacham Winn Culler syndrome722461004
- Meacham syndrome722461004
- Congenital atrophy of optic nerve722990003
- Congenital optic atrophy722990003
- N syndrome723410002
- Dyskeratosis congenita with bilateral exudative retinopathy723512008
- Retinopathy, anaemia, central nervous system anomalies syndrome723512008
- Retinopathy, anemia, central nervous system anomalies syndrome723512008
- Revesz DeBuse syndrome723512008
- Revesz syndrome723512008
- Trichothiodystrophy723551003
- Corneo-dermato-osseous syndrome723584003
- Corneodermatoosseous syndrome723584003
- Stern Lubinsky Durrie syndrome723584003
- Elejalde disease724091002
- Neuroectodermal melanolysosomal disease724091002
- DNA (deoxyribonucleic acid) ligase IV deficiency724177005
- Deoxyribonucleic acid ligase IV deficiency724177005
- LIG4 (ligase 4) syndrome724177005
- LIG4 syndrome724177005
- Ligase 4 syndrome724177005
- Keutel syndrome724208006
- Pulmonic stenosis, brachytelephalangism, calcification of cartilage syndrome724208006
- Crisponi syndrome725097006
- Deletion of part of chromosome 11726381002
- Deletion of part of long arm of chromosome 12726383004
- Dystopia canthorum726407000
- Weaver Williams syndrome726670008
- Marfanoid syndrome De Silva type732262003
- German syndrome733037000
- Alaninuria, microcephaly, dwarfism, enamel hypoplasia, diabetes mellitus syndrome733072002
- Stimmler syndrome733072002
- Absent eyebrows and eyelashes with intellectual disability syndrome733086003
- Hall Berg Rudolph syndrome733086003
- Pseudoprogeria syndrome733086003
- Van den Bosch syndrome733110004
- Carney complex733491005
- Carney syndrome733491005
- LAMB (lentigines, atrial myxoma, blue naevi) syndrome733491005
- LAMB (lentigines, atrial myxoma, blue nevi) syndrome733491005
- Myxoma, spotty pigmentation, endocrine overactivity syndrome733491005
- Gonadal dysgenesis XY type with associated anomalies733605002
- XY type gonadal dysgenesis with associated anomalies syndrome733605002
- Wolfram-like syndrome734022008
- Congenital conductive hearing loss737344003
- Congenital mixed conductive and sensorineural hearing loss737377004
- Developmental delay, hypotonia, extremities hypertrophy syndrome763186006
- Grubben, De Cock, Borghgraef syndrome763186006
- Insulin resistance763325000
- Branchio-otic syndrome764810000
- Branchiootic syndrome764810000
- Birk Barel mental retardation dysmorphism syndrome764861005
- Intellectual disability Birk-Barel type764861005
- Intellectual disability, hypotonia, facial dysmorphism syndrome764861005
- KCNK9 (potassium two pore domain channel subfamily K member 9) imprinting syndrome764861005
- Axial mesodermal dysplasia spectrum765755006
- Blastogenesis defect765755006
- Russell Weaver Bull syndrome765755006
- Carney complex variant766881008
- Carney complex, trismus, pseudocamptodactyly syndrome766881008
- PURA (purine rich element binding protein A) syndrome768473009
- PURA syndrome768473009
- PURA-related neurodevelopmental disorder768473009
- PURA-related severe neonatal hypotonia, seizure, encephalopathy syndrome768473009
- Purine rich element binding protein A syndrome768473009
- Patterson pseudoleprechaunism syndrome771262009
- Patterson syndrome771262009
- Pseudoleprechaunism syndrome Patterson type771262009
- Micro syndrome772224009
- Warburg micro syndrome772224009
- RAB18 deficiency772225005
- RAB18, member RAS oncogene family deficiency772225005
- Chudley McCullough syndrome773610007
- Acrodysplasia scoliosis773773006
- Brachydactyly, scoliosis, carpal fusion syndrome773773006
- Prata Liberal Goncalves syndrome773773006
- Multisystemic smooth muscle dysfunction syndrome782724001
- Congenital lymphangiectases788292004
- Congenital lymphangiectasia788292004
- Congenital lymphangiectasis788292004
- Blepharophimosis, intellectual disability syndrome788584007
- Aortic aneurysm due to Loeys-Dietz syndrome838364007
- Nodular hyperplasia of adrenal cortex874911000
- Adrenal cortical nodule874912007
- Nodule of adrenal cortex874912007
- 11p15 deletion syndrome880078001
- 12q15 deletion syndrome880081006
- 12q24.31-q24.32 deletion syndrome880086001
- Congenital corneal dystrophy1003408005
- Congenital dystrophy of cornea1003408005
- Waardenburg syndrome type 11010606009
- Waardenburg syndrome type I1010606009
- Waardenburg syndrome type 21010636000
- Waardenburg syndrome type II1010636000
- Arginine-glutamic acid dipeptide repeats-related neurodevelopmental syndrome1172624000
- RERE-related neurodevelopmental syndrome1172624000
- Periodontitis exacerbated by Cohen syndrome1184620004
- Apple peel intestinal atresia, ocular anomalies, microcephaly syndrome1187120008
- Jejunal atresia, microcephaly, ocular anomalies syndrome1187120008
- Stromme syndrome1187120008
- LAMA5-related multisystemic syndrome1217370006
- Laminin subunit alpha 5-related multisystemic syndrome1217370006
- Long QT syndrome type 81230096008
- Timothy syndrome1230096008
- Atypical Timothy syndrome1230097004
- Atypical long QT syndrome type 81230097004
- Timothy syndrome atypical type1230097004
- FG syndrome type 11237179007
- Opitz Kaveggia syndrome1237179007
- Hydrops, lactic acidosis, sideroblastic anaemia, multisystemic failure syndrome1237349008
- Hydrops, lactic acidosis, sideroblastic anemia, multisystemic failure syndrome1237349008
- Symptomatic form of Coffin-Lowry syndrome in female carrier1237577000
- Birt Hogg Dubé syndrome1263460007
- Fibrofolliculomas with trichodiscomas and acrochordons1263460007
- Hornstein Knickenberg syndrome1263460007
- Infantile haemangioma1293125002
- Infantile hemangioma1293125002
- KLHL7 (kelch like family member 7) related Bohring Opitz-like syndrome1300133004
- KLHL7-related Bohring Opitz-like syndrome1300133004
- Kelch like family member 7-related Bohring Opitz-like syndrome1300133004
- KLHL7 (kelch like family member 7) related Bohring-Opitz-like and Crisponi/cold-induced sweating-like overlap syndrome1304116002
- KLHL7-related Bohring-Opitz-like and Crisponi/cold-induced sweating-like overlap syndrome1304116002
- Kelch like family member 7-related Bohring-Opitz-like and Crisponi/cold-induced sweating-like overlap syndrome1304116002
- PERCHING syndrome1304116002
- KLHL7 (kelch like family member 7) related Crisponi/cold-induced sweating-like syndrome1304117006
- KLHL7-related Crisponi-like syndrome1304117006
- KLHL7-related Crisponi/cold-induced sweating-like syndrome1304117006
- Kelch like family member 7-related Crisponi/cold-induced sweating-like syndrome1304117006
- Cardiac urogenital syndrome1332387008
- MYRF-related cardiac urogenital syndrome1332387008
- Myelin regulatory factor-related cardiac urogenital syndrome1332387008
- CHD4-related neurodevelopmental disorder1332510002
- CHD4-related neurodevelopmental syndrome1332510002
- Chromodomain helicase DNA binding protein 4-related neurodevelopmental disorder1332510002
- Sifrim Hitz Weiss syndrome1332510002
- Carney complex-associated-primary pigmented nodular adrenocortical disease1348308009
- c-PPNAD - Carney complex-associated-primary pigmented nodular adrenocortical disease1348308009
- PHACES syndrome1351350008
- Posterior fossa brain malformation, haemangioma, arterial anomaly, cardiac defect, aortic coarctation, eye abnormality, sternal anomalies syndrome1351350008
- Posterior fossa brain malformation, hemangioma, arterial anomaly, cardiac defect, aortic coarctation, eye abnormality, sternal anomalies syndrome1351350008
- Developmental delay, behavioral problems, small hands and feet, cyclic vomiting, dysmorphic features syndrome1351655009
- Developmental delay, behavioural problems, small hands and feet, cyclic vomiting, dysmorphic features syndrome1351655009
- JDVS - Jansen-de Vries syndrome1351655009
- Jansen-de Vries syndrome1351655009
- Alkuraya Kucinskas syndrome1351836007
- KIAA1109-related early lethal congenital brain malformations, arthrogryposis syndrome1351836007
- Genetic syndromic childhood obesity1359763002
- Congenital osteodystrophy5731000119108
- Congenital peripheral pulmonary artery stenosis286071000119109
Frequently Asked Questions
What is the ICD-10 code for oth congenital malformation syndromes, nec?
The ICD-10-CM code for oth congenital malformation syndromes, nec is Q87.89. The full clinical description is "Other specified congenital malformation syndromes, not elsewhere classified". Q87.89 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Q87.89 mean?
ICD-10-CM code Q87.89 represents "Other specified congenital malformation syndromes, not elsewhere classified". 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 Q87.89 a billable code?
Yes, Q87.89 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q87.89 in?
Q87.89 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q87.89?
Q87.89 has Excludes1 notes indicating codes that cannot be used together with it, including: Zellweger syndrome (E71.510).
Are additional codes required with Q87.89?
Yes, when using Q87.89 you should also code: code(s) to identify all associated manifestations.
What SNOMED CT codes does Q87.89 map to?
Q87.89 maps to 219 SNOMED CT concepts: 4135001, 880078001, 880081006, 880086001, 303098002, and 214 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q87.89?
Q87.89 is linked to 1 UMLS Concept Unique Identifier: C0869083. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
Automate ICD-10 Coding With AI
Send clinical text to the AutoICD API and get back structured ICD-10 codes with confidence scores. Integrates into any EHR or billing system in minutes.
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.