Diagnosis Code: Q87.89

Short Description: Oth congenital malformation syndromes, NEC

Long Description: Other specified congenital malformation syndromes, not elsewhere classified

The code Q87.89 is VALID for claim submission

Code Classification:

• Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
  • Other congenital malformations (Q80-Q89)
    • Oth congenital malform syndromes affecting multiple systems (Q87)
      • Q87.89 Oth congenital malformation syndromes, NEC

Code Version: 2022 ICD-10-CM

Synonyms

• 11p partial monosomy syndrome
• 11p15 deletion syndrome
• 12q15 deletion syndrome
• 12q24.31-q24.32 deletion syndrome
• 3-Phosphoglycerate dehydrogenase deficiency
• Ablepharon
• Absent eyebrow
• Acrodysplasia scoliosis
• Adrenal hyperfunction
• Allemann's syndrome
• Alstrom syndrome
• Alveolar bone loss
• Andersen Tawil syndrome
• Aortic aneurysm due to Loeys-Dietz syndrome
• Aplasia cutis congenita secondary to malformation syndrome
• Aplasia cutis in Johanson-Blizzard syndrome
• Athetoid movement
• Atypical Timothy syndrome
• Autosomal dominant dyskeratosis congenita
• Autosomal dominant popliteal pterygium syndrome
• Autosomal recessive popliteal pterygium syndrome
• Axial mesodermal dysplasia spectrum
• Bamforth Lazarus syndrome
• Bardet-Biedl syndrome
• Biemond syndrome type 2
• Biemond's syndrome
• Blepharophimosis, intellectual disability syndrome
• Blepharophimosis, intellectual disability syndrome
• Bohring Opitz syndrome
• Bone age finding
• Bosley Salih Alorainy syndrome
• Bowen-Conradi syndrome
• Braddock syndrome
• Branchiootic syndrome
• BSG syndrome
• Cardiocranial syndrome Pfeiffer type
• Carney complex
• Carney complex, trismus, pseudocamptodactyly syndrome
• Choroideremia
• Christianson syndrome
• Chudley McCullough syndrome
• Cohen syndrome
• Cold-induced sweating syndrome
• Congenital absence of eyelash
• Congenital anomaly of lymphatic structure of trunk
• Congenital atresia of external auditory canal
• Congenital atrophy of optic nerve
• Congenital blepharophimosis
• Congenital blepharophimosis
• Congenital coloboma of iris
• Congenital conductive hearing loss
• Congenital corneal dystrophy
• Congenital corneal dystrophy
• Congenital intrauterine infection-like syndrome
• Congenital lymphangiectasia
• Congenital malformation of the eyebrow
• Congenital mixed conductive and sensorineural hearing loss
• Congenital osteodystrophy
• Congenital peripheral pulmonary artery stenosis
• Congenital stenosis of pulmonary artery
• Constitutional aplastic anemia
• Cooper Jabs syndrome
• Costello syndrome
• Craniofacial deafness hand syndrome
• Craniofacial ulnar renal syndrome
• Crisponi syndrome
• Currarino triad
• Cutis laxa, autosomal recessive
• Cutis laxa-corneal clouding-oligophrenia syndrome
• de Barsy syndrome
• Delayed bone age
• Deletion of part of chromosome 11
• Deletion of part of long arm of chromosome 12
• Deletion of part of long arm of chromosome 12
• Developmental malformation of branchial arch
• Developmental malformation, deafness, dystonia syndrome
• DICER1 syndrome
• Disorder of serine metabolism
• Donnai-Barrow syndrome
• Dyskeratosis congenita
• Dystopia canthorum
• Dystrophy of anterior cornea
• Ear, patella, short stature syndrome
• Feingold syndrome
• Fetal acidosis
• Fetal anemia
• FG syndrome
• FG syndrome type 1
• Fixed dilatation of pupil
• Floating-Harbor syndrome
• Francois syndrome
• Fried syndrome
• Generalized dystonia
• German syndrome
• Glucose-galactose malabsorption
• Gomez Lopez Hernandez syndrome
• Grubben, De Cock, Borghgraef syndrome
• Haim Munk syndrome
• Hecht syndrome
• Hennekam syndrome
• Hereditary disorder of lymphatic system
• Heritable pulmonary arterial hypertension
• Hydrops fetalis
• Hydrops, lactic acidosis, sideroblastic anemia, multisystemic failure syndrome
• Hyperreflexia
• Immotile cilia syndrome
• Immotile cilia syndrome due to defective radial spokes
• Insulin resistance
• Intellectual disability Birk-Barel type
• Intestinal lymphangiectasis
• Johnson neuroectodermal syndrome
• Juberg Hayward syndrome
• Keutel syndrome
• Kleefstra syndrome
• LAMA5-related multisystemic syndrome
• Laurence-Moon syndrome
• LIG4 syndrome
• Loeys-Dietz syndrome
• Lowry MacLean syndrome
• Malabsorption of glucose
• Marden Walker syndrome
• Marfanoid physique
• Marfanoid syndrome De Silva type
• Matthew Wood syndrome
• McKusick Kaufman syndrome
• Meacham syndrome
• Metabolic disorder of fetus
• Mixed conductive AND sensorineural hearing loss
• Multiple malformation syndrome with senile-like appearance
• Multiple system malformation syndrome
• Multisystemic smooth muscle dysfunction syndrome
• Myhre syndrome
• Myxoma of heart
• Myxoma of heart
• N syndrome
• Nance-Horan syndrome
• Neu-Laxova syndrome
• Neuroectodermal melanolysosomal disease
• Nicolaides-Baraitser syndrome
• Oculodental syndrome
• Oculodentodigital syndrome
• Oculodento-osseous dysplasia
• Oculodento-osseous dysplasia
• Oculodento-osseous dysplasia - mild type
• Oculodento-osseous dysplasia - severe type
• Oculofaciocardiodental syndrome
• Oculotrichodysplasia
• Ohdo syndrome, Maat-Kievit-Brunner type
• Ohdo syndrome, Say-Barber-Biesecker-Young-Simpson variant
• Oto-onycho-peroneal syndrome
• Pallister-Hall syndrome
• Papillon-Lefèvre syndrome
• Partial ablepharon
• Patent ductus arteriosus
• Pena-Shokeir syndrome type I
• Periodic paralysis
• Periodontitis due to Papillon-Lefèvre syndrome
• Periodontitis exacerbated by Cohen syndrome
• Peripheral pulmonary artery stenosis
• Photosensitivity with ichthyosis, brittle hair, impaired intelligence, decreased fertility and short stature syndrome
• Polyglandular hyperfunction
• Popliteal pterygium syndrome
• Posterior fossa brain malformation, haemaniogma, arterial anomaly, cardiac defect and aortic coarctation, eye abnormality synodrome and sternal anomaly syndrome
• Posterior fossa brain malformation, hemangioma, arterial anomaly, cardiac defect and aortic coarctation, and eye abnormality syndrome
• Primary ciliary dyskinesia and retinitis pigmentosa syndrome
• Primary ciliary dyskinesia due to transposition of ciliary microtubules
• Pseudoleprechaunism syndrome Patterson type
• Pseudoprogeria syndrome
• PURA syndrome
• Pure gonadal dysgenesis
• Pure gonadal dysgenesis 46,XY
• RAB18 deficiency
• RAB18 deficiency
• Renpenning syndrome
• RERE-related neurodevelopmental syndrome
• Revesz syndrome
• Rhombencephalosynapsis
• Rutland ciliary disorientation syndrome
• Scholte syndrome
• Schöpf-Schulz-Passarge syndrome
• Sensory hearing loss
• Severe combined immunodeficiency with low T- and B-cell numbers
• Severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome
• Siegler Brewer Carey syndrome
• Singleton-Merten syndrome
• Snyder-Robinson syndrome
• Speech delay
• Stern Lubinsky Durrie syndrome
• Stimmler syndrome
• Stromme syndrome
• Symptomatic form of Coffin-Lowry syndrome in female carrier
• Timothy syndrome
• Timothy syndrome
• Timothy syndrome type 1
• Trichothiodystrophy
• VACTEL syndrome
• Van den Bosch syndrome
• Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, renal anomalies, limb defects syndrome
• Vici syndrome
• Waardenburg syndrome
• Waardenburg syndrome
• Waardenburg syndrome type 1
• Waardenburg syndrome type 2
• Warburg micro syndrome
• Weaver Williams syndrome
• Wolfram-like syndrome
• X-linked intellectual disability Armfield type
• X-linked intellectual disability Pai type
• X-linked retinitis pigmentosa
• XY type gonadal dysgenesis with associated anomalies syndrome
• Young's syndrome
• Zimmermann-Laband syndrome

Diagnostic Related Group(s)

The code Q87.89 is grouped in the following Diagnostic Related Group(s) (MS-DRG v39.0)

• Other Musculoskeletal System And Connective Tissue Diagnoses With Mcc (564)
• Other Musculoskeletal System And Connective Tissue Diagnoses With Cc (565)
• Other Musculoskeletal System And Connective Tissue Diagnoses Without Cc/mcc (566)

Crosswalk Information

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This page was last updated on: 10/1/2023

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