Q89.89 OTHER SPECIFIED CONGENITAL MALFORMATIONS

Synonyms

• Abnormal communication between pericardial sac and peritoneal cavity
• Abnormal fetal duplication
• Acardia
• Acardia
• Acephalobrachius
• Acephalogaster
• Aggressive fibromatosis of abdomen
• Aggressive infantile fibromatosis
• Aggressive systemic infantile myofibromatosis
• Amniotic adhesion
• Aplasia cutis congenita due to underlying malformation
• Aplasia of lymphatic vessel
• 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 pulmonary lymphatic dysplasia syndrome
• Congenital short trunk
• Derencephalus
• Developmental malformation of branchial arch
• Dicheirus
• Diprosopus
• Diprosopus tetrophthalmus
• Disproportionate short stature
• 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
• Lethal congenital disproportionate short trunk short stature
• 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
• Myofibromatosis
• Myofibromatosis
• Myofibromatosis
• Myofibromatosis
• 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 Q89.89 is grouped in the following Diagnostic Related Group(s) MS-DRG V43.0

1. Other Musculoskeletal System And Connective Tissue Diagnoses With Mcc (564)
2. Other Musculoskeletal System And Connective Tissue Diagnoses With Cc (565)
3. Other Musculoskeletal System And Connective Tissue Diagnoses Without Cc/mcc (566)

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