Diagnosis Code: Q89.8

Short Description: Other specified congenital malformations

Long Description: Other specified congenital malformations

The code Q89.8 is VALID for claim submission

Code Classification:

• Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
  • Other congenital malformations (Q80-Q89)
    • Other congenital malformations, not elsewhere classified (Q89)
      • Q89.8 Other specified congenital malformations

Code Version: 2022 ICD-10-CM

Synonyms

• Abdominal fibromatosis
• Abnormal communication between pericardial sac and peritoneal cavity
• Abnormal fetal duplication
• Acardia
• Acardia
• Acephalobrachius
• Acephalogaster
• Aggressive fibromatosis
• Aggressive fibromatosis
• Aggressive infantile fibromatosis
• Aggressive systemic infantile myofibromatosis
• Amniotic adhesion
• Aplasia cutis congenita due to underlying malformation
• Borjeson-Forssman-Lehmann syndrome
• Cardiac anomaly and heterotaxy syndrome
• Celosomus
• Cephalodiprosopus
• CHARGE syndrome
• Coffin-Lowry syndrome
• Congenital absence of stomach
• Congenital anomaly of body cavity
• Congenital anomaly of body cavity
• Congenital anomaly of body wall
• Congenital anomaly of lower trunk
• Congenital anomaly of lymphatic structure of trunk
• Congenital anomaly of peritoneum
• Congenital anomaly of trunk
• Congenital anomaly of upper trunk
• Congenital deformity of soft tissue
• Congenital flat back deformity
• Congenital hemihypertrophy
• Congenital malformation of lymphatic system of cervicofacial region
• Congenital malformation of lymphatic vessel of skin
• Congenital malformation of vitreous humor
• Congenital malformation of vitreous humor
• Congenital malformation of vitreous humor
• Congenital malformation of vitreous humor
• Congenital pulmonary lymphatic dysplasia syndrome
• Congenital short trunk
• Derencephalus
• Developmental malformation of branchial arch
• Dicheirus
• Diprosopus
• Diprosopus tetrophthalmus
• Duplication of upper limb
• Dysplasia of lung
• Embryological remnant
• Hereditary disorder of lymphatic system
• Hereditary hyperekplexia
• Hereditary vitreoretinopathy
• Hereditary vitreoretinopathy
• Hereditary vitreoretinopathy
• Hereditary vitreoretinopathy
• Holoacardius acephalus
• Holoacardius amorphus
• Hyperekplexia epilepsy syndrome
• Hyperexplexia
• Hyperexplexia
• Hyperexplexia
• Infantile myofibromatosis
• Kabuki make-up syndrome
• Lymphatic malformation
• Marfanoid physique
• Mixed cystic lymphatic malformation
• Monocephalus
• Monocephalus tetrapus dibrachius
• Mullerian duct and limb anomalies syndrome
• Mullerian remnant
• Multicentric infantile myofibromatosis
• Multifocal lymphangioendotheliomatosis, thrombocytopenia syndrome
• Odontotrichomelic syndrome
• Omphaloangiopagus
• Parasitic twin of asymmetrical conjoined twins
• Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease
• Persistent Müllerian duct syndrome
• PTEN hamartoma tumor syndrome
• Pygomelus
• Segmental outgrowth, lipomatosis, arteriovenous malformation, epidermal nevus syndrome
• Shprintzen Goldberg craniosynostosis syndrome
• Simonart's band
• Situs ambiguus
• Situs ambiguus
• Solitary infantile myofibromatosis
• Stickler syndrome
• Stickler syndrome type 1
• Stickler syndrome type 2
• Stickler syndrome type 3
• Stickler syndrome type 4
• Thoracodidymus
• Waardenburg Shah syndrome
• Waardenburg syndrome
• Waardenburg syndrome
• Waardenburg syndrome

Diagnostic Related Group(s)

The code Q89.8 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)

References to Index of Diseases and Injuries

The code Q89.8 has the following ICD-10-CM references to the Index of Diseases and Injuries

Crosswalk Information

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

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