Q87.89 de Barsy syndrome

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de Barsy syndrome

de Barsy syndrome
Synonym for Other specified congenital malformation syndromes, not elsewhere classified

    Q00-Q99 Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)|Q80-Q89 Other congenital malformations (Q80-Q89)|Q87 Other specified congenital malformation syndromes affecting multiple systems|Q87.8 Other specified congenital malformation syndromes, not elsewhere classified

Results for de Barsy syndrome and additional synonyms


Q87.89
Other specified congenital malformation syndromes, not elsewhere classified

Synonyms:

Allemann syndrome|Allemann's syndrome|Allemann's syndrome (disorder)|Alstrom syndrome|Alstrom syndrome (disorder)|Andersen Tawil syndrome|Andersen Tawil syndrome (disorder)|Andersen cardiodysrhythmic periodic paralysis|Aplasia cutis congenita secondary to malformation syndrome (Type 9)|Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder)|Aplasia cutis in Johanson-Blizzard syndrome|Aplasia cutis in Johanson-Blizzard syndrome (disorder)|Arthrocutaneouveal granulamotosis|Azoospermia, obstructive and chronic sinopulmonary infections|Bardet-Biedl syndrome|Bardet-Biedl syndrome (disorder)|Barry-Perkins-Young syndrome|Biedl-Bardet syndrome|Biemond syndrome|Biemond's syndrome|Biemond's syndrome (disorder)|Blau syndrome|Blepharophimosis-intellectual deficit syndrome, Say-Barber/Biesecker/Young-Simpson type|Blepharophimosis-mental retardation syndrome, Maat-Kievit-Brunner type|Blepharophimosis-mental retardation syndrome, Maat-Kievit-Brunner type (disorder)|Blepharophimosis-mental retardation syndrome, Say-Barber-Biesecker-Young-Simpson type|Blepharophimosis-mental retardation syndrome, Say-Barber-Biesecker-Young-Simpson type (disorder)|Bowen Hutterite syndrome|Bowen-Conradi Hutterite syndrome|Bowen-Conradi syndrome|Bowen-Conradi syndrome (disorder)|Christianson syndrome|Cohen syndrome|Cohen syndrome (disorder)|Costello syndrome|Costello syndrome (disorder)|Craniofacial deafness hand syndrome|Craniofacial deafness hand syndrome (disorder)|Curtius' syndrome I|Cutis laxa, corneal clouding AND mental retardation|Cutis laxa-corneal clouding-oligophrenia syndrome|Cutis laxa-corneal clouding-oligophrenia syndrome (disorder)|DICER1 syndrome|Diaphragmatic hernia-exomphalos-corpus callosum agenesis|Diaphragmatic hernia-exomphalos-hypertelorism syndrome|Diaphragmatic hernia-exomphalos-hypertelorism syndrome (disorder)|Donnai-Barrow syndrome|Dysmotile cilia syndrome|Ear, patella, short stature syndrome|Ear, patella, short stature syndrome (disorder)|Early onset sarcoidosis|Facial dysmorphism, intellectual deficit, short stature and hearing loss|Facio-genito-popliteal syndrome|Faciooculoacousticorenal syndrome|Familial granulomatosis, Blau type|Familial granulomatous inflammatory arthritis, dermatitis and uveitis|Familial granulomatous inflammatory arthritis, dermatitis and uveitis (disorder)|Familial juvenile systemic granulomatosis|Feingold syndrome|Fetal akinesia-hypokinesia sequence|Foetal akinesia-hypokinesia sequence|Golabi-Ito-Hall syndrome|Granulomatous inflammatory arthritis, dermatitis and uveitis, familial|Hamel cerebropalatocardiac syndrome|Hard E syndrome|Hecht syndrome|Hecht syndrome (disorder)|Hennekam lymphangiectasia-lymphedema syndrome|Hennekam lymphangiectasia-lymphedema syndrome (disorder)|Hennekam lymphangiectasia-lymphoedema syndrome|Hutterite syndrome|Hydrometrocolpos, postaxial polydactyly, and congenital heart malformation|Hydrometrocolpos, postaxial polydactyly, and congenital heart malformation (disorder)|ICS - Immotile cilia syndrome|Immotile cilia syndrome|Immotile cilia syndrome (disorder)|Immotile cilia syndrome due to defective radial spokes|Immotile cilia syndrome due to defective radial spokes (disorder)|Jackson-Weiss syndrome|Jackson-Weiss syndrome (disorder)|Juvenile periodontosis with hyperkeratosis|LMBB - Laurence-Moon-Bardet-Biedl syndrome|Laband-Zimmermann syndrome|Laryngotracheal stenosis, arthropathy, prognathism and short stature|Laurence-Moon (-Bardet)-Biedl syndrome|Laurence-Moon syndrome|Laurence-Moon syndrome (disorder)|Laurence-Moon-Biedl syndrome|Long QT syndrome 7|Long QT syndrome with syndactyly|Marden Walker syndrome|Marden Walker syndrome (disorder)|McKusick Kaufman syndrome|Meier-Gorlin syndrome|Mental retardation, x-linked, Snyder-Robinson type|Microcephaly-mesobrachyphalangy-tracheoesophageal fistula syndrome|Microcephaly-oculo-digito-esophageal-duodenal syndrome|Microcephaly-oculo-digito-esophageal-duodenal syndrome (disorder)|Microcephaly-oculo-digito-oesophageal-duodenal syndrome|Microphthalmia syndromic 2|Microphthalmia, cataract, radiculomegaly and septal heart defect|Microtia, absent patellae, micrognathia syndrome|Multiple malformation syndrome with senile-like appearance|Multiple malformation syndrome with senile-like appearance (disorder)|Multiple system malformation syndrome|Multiple system malformation syndrome (disorder)|Myhre syndrome|Myhre syndrome (disorder)|NLS - Neu-Laxova syndrome|Nance-Horan syndrome|Nance-Horan syndrome (disorder)|Neu-Laxova syndrome|Neu-Laxova syndrome (disorder)|Oculo-digito-esophagoduodenal syndrome|Oculo-digito-oesophagoduodenal syndrome|Oculo-facio-cardio-dental syndrome|Oculodental syndrome|Oculodental syndrome (disorder)|Oculodento-osseous dysplasia - mild type|Oculodento-osseous dysplasia - mild type (disorder)|Oculodento-osseous dysplasia - severe type|Oculodento-osseous dysplasia - severe type (disorder)|Oculodentodigital dysplasia|Oculodentodigital syndrome|Oculodentodigital syndrome (disorder)|Oculofaciocardiodental syndrome|Oculofaciocardiodental syndrome (disorder)|Ohdo syndrome, Maat-Kievit-Brunner type|Ohdo syndrome, Say-Barber-Biesecker-Young-Simpson variant|Oto-onycho-peroneal syndrome|Oto-onycho-peroneal syndrome (disorder)|PCD - Primary ciliary dyskinesia|PHACE (Posterior fossa brain malformation, hemangioma, arterial anomaly, cardiac defect and aortic coarctation, and eye abnormality) syndrome|PHACES (Posterior fossa brain malformation, haemaniogma, arterial anomaly, cardiac defect and aortic coarctation, eye abnormality synodrome and sternal anomaly) syndrome|PIBIDS syndrome, photosensitivity with IBIDS|Pallister-Hall syndrome|Pallister-Hall syndrome (disorder)|Papillon-Lefevre syndrome|Papillon-Lefèvre syndrome|Papillon-Lefèvre syndrome (disorder)|Pediatric granulomatous arthritis|Pena-Shokeir syndrome type I|Pena-Shokeir syndrome type I (disorder)|Periodontitis due to Papillon-Lefevre syndrome|Periodontitis due to Papillon-Lefèvre syndrome|Periodontitis due to Papillon-Lefèvre syndrome (disorder)|Photosensitivity with ichthyosis, brittle hair, impaired intelligence, decreased fertility and short stature syndrome|Photosensitivity with ichthyosis, brittle hair, impaired intelligence, decreased fertility and short stature syndrome (disorder)|Pleuropulmonary blastoma familial tumor and dysplasia syndrome|Pleuropulmonary blastoma familial tumour and dysplasia syndrome|Pleuropulmonary blastoma family tumor susceptibility syndrome|Pleuropulmonary blastoma family tumor susceptibility syndrome (disorder)|Pleuropulmonary blastoma family tumour susceptibility syndrome|Polynesian bronchiectasis|Popliteal pterygium syndrome|Popliteal pterygium syndrome (disorder)|Porteous syndrome|Posterior fossa brain malformation, haemangioma, arterial anomaly, cardiac defect and aortic coarctation, and eye abnormality syndrome|Posterior fossa brain malformation, haemaniogma, arterial anomaly, cardiac defect and aortic coarctation, eye abnormality synodrome and sternal anomaly syndrome|Posterior fossa brain malformation, haemaniogma, arterial anomaly, cardiac defect and aortic coarctation, eye abnormality synodrome and sternal anomaly syndrome (disorder)|Posterior fossa brain malformation, hemangioma, arterial anomaly, cardiac defect and aortic coarctation, and eye abnormality syndrome|Posterior fossa brain malformation, hemangioma, arterial anomaly, cardiac defect and aortic coarctation, and eye abnormality syndrome (disorder)|Primary ciliary dyskinesia|Primary ciliary dyskinesia due to transposition of ciliary microtubules|Primary ciliary dyskinesia due to transposition of ciliary microtubules (disorder)|Progeroid syndrome of de Barsey|Renpenning syndrome|Renpenning syndrome (disorder)|Rutherfurd syndrome|Rutland ciliary disorientation syndrome|Rutland ciliary disorientation syndrome (disorder)|Say-Barber-Biesecker-Young-Simpson syndrome|Say-Barber-Biesecker-Young-Simpson variant of Ohdo syndrome|Schöpf-Schulz-Passarge syndrome|Schöpf-Schulz-Passarge syndrome (disorder)|Singleton-Merten syndrome|Singleton-Merten syndrome (disorder)|Sinusitis-infertility syndrome|Snyder-Robinson syndrome|Snyder-Robinson x-linked mental retardation syndrome|Snyder-Robinson x-linked mental retardation syndrome (disorder)|Sutherland-Haan syndrome|Timothy syndrome classic type|Timothy syndrome type 1|Timothy syndrome type 1 (disorder)|Trismus pseudocamptodactyly syndrome|VACTEL syndrome|Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, limb defects (VACTEL) syndrome|Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, limb defects syndrome|Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, limb defects syndrome (disorder)|Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, renal anomalies, limb defects (VACTERL) syndrome|Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, renal anomalies, limb defects syndrome|Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, renal anomalies, limb defects syndrome (disorder)|Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-oesophageal fistula, renal anomalies, limb defects (VACTERL) syndrome|Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-oesophageal fistula, renal anomalies, limb defects syndrome|Warburg syndrome|Warburg syndrome (disorder)|X-linked Ohdo syndrome|X-linked intellectual deficit due to PQBP1 mutation|X-linked intellectual deficit, South African type|X-linked mental retardation syndrome, Christianson type|X-linked mental retardation syndrome, Christianson type (disorder)|Young syndrome|Young's syndrome|Young's syndrome (disorder)|Young-Simpson syndrome|Zimmermann-Laband syndrome|Zimmermann-Laband syndrome (disorder)|de Barsey syndrome|de Barsey-Moens-Dierckx syndrome|de Barsy syndrome|de Barsy syndrome (disorder)

Subcategories:

    All content of the ICD-10 CM Search is based on the classifications and codes of the Centers for Medicare and Medicaid Services (CMS) and the National Center for Health Statistics (NCHS). The accumulation of synonyms is carried out by Averbis GmbH with Healthcare Natural Language Processing. All information is provided without guarantee. Errors and omissions excepted. We expressly reserve the right to make changes, additions or deletions to the information or links provided at any time without prior notice. Our offer is non-binding. For correctness, completeness and topicality or designations no liability is assumed.

    ICD-Search ICD 10 CM (Clinical Modification) 2017 through Healthcare Natural Language Processing & Deep Learning

    ICD-Code / International Statistical Classification of Diseases and Related Health Problems (ICD) for: de Barsy syndrome

    ICD Code for Disease, Diagnosis Q87.89

    ICD Code an Classification Other specified congenital malformation syndromes, not elsewhere classified

    Chapter, Outline, Main Categories, Parent Concepts or Top Concepts: Q00-Q99 Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)|Q80-Q89 Other congenital malformations (Q80-Q89)|Q87 Other specified congenital malformation syndromes affecting multiple systems|Q87.8 Other specified congenital malformation syndromes, not elsewhere classified

    Subcategories, subconcepts or child concepts:

    Synonyms:

    Synonyms: Q87.89: de Barsy syndrome

    Other Synonyms of the Category: Allemann syndrome|Allemann's syndrome|Allemann's syndrome (disorder)|Alstrom syndrome|Alstrom syndrome (disorder)|Andersen Tawil syndrome|Andersen Tawil syndrome (disorder)|Andersen cardiodysrhythmic periodic paralysis|Aplasia cutis congenita secondary to malformation syndrome (Type 9)|Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder)|Aplasia cutis in Johanson-Blizzard syndrome|Aplasia cutis in Johanson-Blizzard syndrome (disorder)|Arthrocutaneouveal granulamotosis|Azoospermia, obstructive and chronic sinopulmonary infections|Bardet-Biedl syndrome|Bardet-Biedl syndrome (disorder)|Barry-Perkins-Young syndrome|Biedl-Bardet syndrome|Biemond syndrome|Biemond's syndrome|Biemond's syndrome (disorder)|Blau syndrome|Blepharophimosis-intellectual deficit syndrome, Say-Barber/Biesecker/Young-Simpson type|Blepharophimosis-mental retardation syndrome, Maat-Kievit-Brunner type|Blepharophimosis-mental retardation syndrome, Maat-Kievit-Brunner type (disorder)|Blepharophimosis-mental retardation syndrome, Say-Barber-Biesecker-Young-Simpson type|Blepharophimosis-mental retardation syndrome, Say-Barber-Biesecker-Young-Simpson type (disorder)|Bowen Hutterite syndrome|Bowen-Conradi Hutterite syndrome|Bowen-Conradi syndrome|Bowen-Conradi syndrome (disorder)|Christianson syndrome|Cohen syndrome|Cohen syndrome (disorder)|Costello syndrome|Costello syndrome (disorder)|Craniofacial deafness hand syndrome|Craniofacial deafness hand syndrome (disorder)|Curtius' syndrome I|Cutis laxa, corneal clouding AND mental retardation|Cutis laxa-corneal clouding-oligophrenia syndrome|Cutis laxa-corneal clouding-oligophrenia syndrome (disorder)|DICER1 syndrome|Diaphragmatic hernia-exomphalos-corpus callosum agenesis|Diaphragmatic hernia-exomphalos-hypertelorism syndrome|Diaphragmatic hernia-exomphalos-hypertelorism syndrome (disorder)|Donnai-Barrow syndrome|Dysmotile cilia syndrome|Ear, patella, short stature syndrome|Ear, patella, short stature syndrome (disorder)|Early onset sarcoidosis|Facial dysmorphism, intellectual deficit, short stature and hearing loss|Facio-genito-popliteal syndrome|Faciooculoacousticorenal syndrome|Familial granulomatosis, Blau type|Familial granulomatous inflammatory arthritis, dermatitis and uveitis|Familial granulomatous inflammatory arthritis, dermatitis and uveitis (disorder)|Familial juvenile systemic granulomatosis|Feingold syndrome|Fetal akinesia-hypokinesia sequence|Foetal akinesia-hypokinesia sequence|Golabi-Ito-Hall syndrome|Granulomatous inflammatory arthritis, dermatitis and uveitis, familial|Hamel cerebropalatocardiac syndrome|Hard E syndrome|Hecht syndrome|Hecht syndrome (disorder)|Hennekam lymphangiectasia-lymphedema syndrome|Hennekam lymphangiectasia-lymphedema syndrome (disorder)|Hennekam lymphangiectasia-lymphoedema syndrome|Hutterite syndrome|Hydrometrocolpos, postaxial polydactyly, and congenital heart malformation|Hydrometrocolpos, postaxial polydactyly, and congenital heart malformation (disorder)|ICS - Immotile cilia syndrome|Immotile cilia syndrome|Immotile cilia syndrome (disorder)|Immotile cilia syndrome due to defective radial spokes|Immotile cilia syndrome due to defective radial spokes (disorder)|Jackson-Weiss syndrome|Jackson-Weiss syndrome (disorder)|Juvenile periodontosis with hyperkeratosis|LMBB - Laurence-Moon-Bardet-Biedl syndrome|Laband-Zimmermann syndrome|Laryngotracheal stenosis, arthropathy, prognathism and short stature|Laurence-Moon (-Bardet)-Biedl syndrome|Laurence-Moon syndrome|Laurence-Moon syndrome (disorder)|Laurence-Moon-Biedl syndrome|Long QT syndrome 7|Long QT syndrome with syndactyly|Marden Walker syndrome|Marden Walker syndrome (disorder)|McKusick Kaufman syndrome|Meier-Gorlin syndrome|Mental retardation, x-linked, Snyder-Robinson type|Microcephaly-mesobrachyphalangy-tracheoesophageal fistula syndrome|Microcephaly-oculo-digito-esophageal-duodenal syndrome|Microcephaly-oculo-digito-esophageal-duodenal syndrome (disorder)|Microcephaly-oculo-digito-oesophageal-duodenal syndrome|Microphthalmia syndromic 2|Microphthalmia, cataract, radiculomegaly and septal heart defect|Microtia, absent patellae, micrognathia syndrome|Multiple malformation syndrome with senile-like appearance|Multiple malformation syndrome with senile-like appearance (disorder)|Multiple system malformation syndrome|Multiple system malformation syndrome (disorder)|Myhre syndrome|Myhre syndrome (disorder)|NLS - Neu-Laxova syndrome|Nance-Horan syndrome|Nance-Horan syndrome (disorder)|Neu-Laxova syndrome|Neu-Laxova syndrome (disorder)|Oculo-digito-esophagoduodenal syndrome|Oculo-digito-oesophagoduodenal syndrome|Oculo-facio-cardio-dental syndrome|Oculodental syndrome|Oculodental syndrome (disorder)|Oculodento-osseous dysplasia - mild type|Oculodento-osseous dysplasia - mild type (disorder)|Oculodento-osseous dysplasia - severe type|Oculodento-osseous dysplasia - severe type (disorder)|Oculodentodigital dysplasia|Oculodentodigital syndrome|Oculodentodigital syndrome (disorder)|Oculofaciocardiodental syndrome|Oculofaciocardiodental syndrome (disorder)|Ohdo syndrome, Maat-Kievit-Brunner type|Ohdo syndrome, Say-Barber-Biesecker-Young-Simpson variant|Oto-onycho-peroneal syndrome|Oto-onycho-peroneal syndrome (disorder)|PCD - Primary ciliary dyskinesia|PHACE (Posterior fossa brain malformation, hemangioma, arterial anomaly, cardiac defect and aortic coarctation, and eye abnormality) syndrome|PHACES (Posterior fossa brain malformation, haemaniogma, arterial anomaly, cardiac defect and aortic coarctation, eye abnormality synodrome and sternal anomaly) syndrome|PIBIDS syndrome, photosensitivity with IBIDS|Pallister-Hall syndrome|Pallister-Hall syndrome (disorder)|Papillon-Lefevre syndrome|Papillon-Lefèvre syndrome|Papillon-Lefèvre syndrome (disorder)|Pediatric granulomatous arthritis|Pena-Shokeir syndrome type I|Pena-Shokeir syndrome type I (disorder)|Periodontitis due to Papillon-Lefevre syndrome|Periodontitis due to Papillon-Lefèvre syndrome|Periodontitis due to Papillon-Lefèvre syndrome (disorder)|Photosensitivity with ichthyosis, brittle hair, impaired intelligence, decreased fertility and short stature syndrome|Photosensitivity with ichthyosis, brittle hair, impaired intelligence, decreased fertility and short stature syndrome (disorder)|Pleuropulmonary blastoma familial tumor and dysplasia syndrome|Pleuropulmonary blastoma familial tumour and dysplasia syndrome|Pleuropulmonary blastoma family tumor susceptibility syndrome|Pleuropulmonary blastoma family tumor susceptibility syndrome (disorder)|Pleuropulmonary blastoma family tumour susceptibility syndrome|Polynesian bronchiectasis|Popliteal pterygium syndrome|Popliteal pterygium syndrome (disorder)|Porteous syndrome|Posterior fossa brain malformation, haemangioma, arterial anomaly, cardiac defect and aortic coarctation, and eye abnormality syndrome|Posterior fossa brain malformation, haemaniogma, arterial anomaly, cardiac defect and aortic coarctation, eye abnormality synodrome and sternal anomaly syndrome|Posterior fossa brain malformation, haemaniogma, arterial anomaly, cardiac defect and aortic coarctation, eye abnormality synodrome and sternal anomaly syndrome (disorder)|Posterior fossa brain malformation, hemangioma, arterial anomaly, cardiac defect and aortic coarctation, and eye abnormality syndrome|Posterior fossa brain malformation, hemangioma, arterial anomaly, cardiac defect and aortic coarctation, and eye abnormality syndrome (disorder)|Primary ciliary dyskinesia|Primary ciliary dyskinesia due to transposition of ciliary microtubules|Primary ciliary dyskinesia due to transposition of ciliary microtubules (disorder)|Progeroid syndrome of de Barsey|Renpenning syndrome|Renpenning syndrome (disorder)|Rutherfurd syndrome|Rutland ciliary disorientation syndrome|Rutland ciliary disorientation syndrome (disorder)|Say-Barber-Biesecker-Young-Simpson syndrome|Say-Barber-Biesecker-Young-Simpson variant of Ohdo syndrome|Schöpf-Schulz-Passarge syndrome|Schöpf-Schulz-Passarge syndrome (disorder)|Singleton-Merten syndrome|Singleton-Merten syndrome (disorder)|Sinusitis-infertility syndrome|Snyder-Robinson syndrome|Snyder-Robinson x-linked mental retardation syndrome|Snyder-Robinson x-linked mental retardation syndrome (disorder)|Sutherland-Haan syndrome|Timothy syndrome classic type|Timothy syndrome type 1|Timothy syndrome type 1 (disorder)|Trismus pseudocamptodactyly syndrome|VACTEL syndrome|Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, limb defects (VACTEL) syndrome|Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, limb defects syndrome|Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, limb defects syndrome (disorder)|Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, renal anomalies, limb defects (VACTERL) syndrome|Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, renal anomalies, limb defects syndrome|Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, renal anomalies, limb defects syndrome (disorder)|Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-oesophageal fistula, renal anomalies, limb defects (VACTERL) syndrome|Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-oesophageal fistula, renal anomalies, limb defects syndrome|Warburg syndrome|Warburg syndrome (disorder)|X-linked Ohdo syndrome|X-linked intellectual deficit due to PQBP1 mutation|X-linked intellectual deficit, South African type|X-linked mental retardation syndrome, Christianson type|X-linked mental retardation syndrome, Christianson type (disorder)|Young syndrome|Young's syndrome|Young's syndrome (disorder)|Young-Simpson syndrome|Zimmermann-Laband syndrome|Zimmermann-Laband syndrome (disorder)|de Barsey syndrome|de Barsey-Moens-Dierckx syndrome|de Barsy syndrome|de Barsy syndrome (disorder)

    ICD 10 CM 2017, (Clinical Modification) for coding of death certificates and mortality data. The international Statistical Classification of Diseases and Related Health Problems (ICD) 10th Revision and Clinical Modification. International Classification of Diseases, Tenth Revision, Clinical Modification.Q87.89 Other specified congenital malformation syndromes, not elsewhere classified and de Barsy syndrome

    de Barsy syndrome
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