 Q89 |
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Other congenital malformations, not elsewhere classified  |
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| Q89.0 |
 |
Congenital absence and malformations of spleen |
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| Excludes1 |
isomerism of atrial appendages (with asplenia or polysplenia) (Q20.6)
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|
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 Q89.01 |
|
Asplenia (congenital) |
| | |
| Q89.09 |
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Congenital malformations of spleen |
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| Q89.1 |
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Congenital malformations of adrenal gland |
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| Excludes1 |
adrenogenital disorders (E25.-)
congenital adrenal hyperplasia (E25.0)
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| Q89.2 |
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Congenital malformations of other endocrine glands |
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| Congenital malformation of parathyroid or thyroid gland | | Persistent thyroglossal duct | | Thyroglossal cyst |
| Excludes1 |
congenital goiter (E03.0)
congenital hypothyroidism (E03.1)
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| Q89.3 |
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Situs inversus |
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| Dextrocardia with situs inversus | | Mirror-image atrial arrangement with situs inversus | | Situs inversus or transversus abdominalis | | Situs inversus or transversus thoracis | | Transposition of abdominal viscera | | Transposition of thoracic viscera |
| Excludes1 |
dextrocardia NOS (Q24.0)
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|
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| Q89.4 |
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Conjoined twins |
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| Craniopagus | | Dicephaly | | Pygopagus | | Thoracopagus |
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|
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| Q89.7 |
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Multiple congenital malformations, not elsewhere classified |
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| Multiple congenital anomalies NOS | | Multiple congenital deformities NOS |
| Excludes1 |
congenital malformation syndromes affecting multiple systems (Q87.-)
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| Q89.8 |
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Other specified congenital malformations |
| |
| UseAdditionalCode |
code(s) to identify all associated manifestations
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| Q89.81 |
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Kabuki syndrome |
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| Kabuki syndrome, type 1, due to KMT2D mutation | | Kabuki syndrome, type 2, due to KDM6A mutation | | Niikawa-Kuroki syndrome |
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| | |
| Q89.89 |
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Other specified congenital malformations |
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| Q89.9 |
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Congenital malformation, unspecified |
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| Congenital anomaly NOS | | Congenital deformity NOS |
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