Other and unspecified congenital anomalies
759
Congenital Anomalies
Both
756-759.99
ICD mappings
| ICD code | Type | Description | Phenome |
|---|---|---|---|
| E78.71 | ICD10CM | Barth syndrome | MGI |
| E78.72 | ICD10CM | Smith-Lemli-Opitz syndrome | MGI |
| M04.2 | ICD10CM | Cryopyrin-associated periodic syndromes | MGI |
| M04.8 | ICD10CM | Other autoinflammatory syndromes | MGI |
| Q85.1 | ICD10CM | Tuberous sclerosis | MGI |
| Q85.8 | ICD10CM | Other phakomatoses, not elsewhere classified | MGI |
| Q85.9 | ICD10CM | Phakomatosis, unspecified | MGI |
| Q87.2 | ICD10CM | Congenital malformation syndromes predominantly involving limbs | MGI |
| Q87.3 | ICD10CM | Congenital malformation syndromes involving early overgrowth | MGI |
| Q87.5 | ICD10CM | Other congenital malformation syndromes with other skeletal changes | MGI |
| Q87.8 | ICD10CM | Other specified congenital malformation syndromes, not elsewhere classified | MGI |
| Q87.81 | ICD10CM | Alport syndrome | MGI |
| Q87.82 | ICD10CM | Arterial tortuosity syndrome | MGI |
| Q87.89 | ICD10CM | Other specified congenital malformation syndromes, not elsewhere classified | MGI |
| Q89.0 | ICD10CM | Congenital absence and malformations of spleen | MGI |
| Q89.01 | ICD10CM | Asplenia (congenital) | MGI |
| Q89.09 | ICD10CM | Congenital malformations of spleen | MGI |
| Q89.1 | ICD10CM | Congenital malformations of adrenal gland | MGI |
| Q89.2 | ICD10CM | Congenital malformations of other endocrine glands | MGI |
| Q89.3 | ICD10CM | Situs inversus | MGI |
| Q89.4 | ICD10CM | Conjoined twins | MGI |
| Q89.7 | ICD10CM | Multiple congenital malformations, not elsewhere classified | MGI |
| Q89.8 | ICD10CM | Other specified congenital malformations | MGI |
| Q89.9 | ICD10CM | Congenital malformation, unspecified | MGI |
| 759.0 | ICD9CM | Anomalies of spleen | MGI |
| 759.1 | ICD9CM | Anomalies of adrenal gland | MGI |
| 759.2 | ICD9CM | Anomalies of other endocrine glands | MGI |
| 759.3 | ICD9CM | Situs inversus | MGI |
| 759.4 | ICD9CM | Conjoined twins | MGI |
| 759.5 | ICD9CM | Tuberous sclerosis | MGI |
| 759.6 | ICD9CM | Other hamartoses, not elsewhere classified | MGI |
| 759.7 | ICD9CM | Multiple congenital anomalies, so described | MGI |
| 759.89 | ICD9CM | Other specified congenital anomalies | MGI |
| 759.9 | ICD9CM | Congenital anomaly, unspecified | MGI |
| 795.2 | ICD9CM | Nonspecific abnormal findings on chromosomal analysis | MGI |
| V13.69 | ICD9CM | Personal history of other (corrected) congenital malformations | MGI |
| Q85.1 | ICD10 | Q85.1 Tuberous sclerosis | UKB |
| Q85.8 | ICD10 | Q85.8 Other phakomatoses, not elsewhere classified | UKB |
| Q85.9 | ICD10 | Q85.9 Phakomatosis, unspecified | UKB |
| Q87.2 | ICD10 | Q87.2 Congenital malformation syndromes predominantly involving limbs | UKB |
| Q87.3 | ICD10 | Q87.3 Congenital malformation syndromes involving early overgrowth | UKB |
| Q87.5 | ICD10 | Q87.5 Other congenital malformation syndromes with other skeletal changes | UKB |
| Q87.8 | ICD10 | Q87.8 Other specified congenital malformation syndromes, not elsewhere classified | UKB |
| Q89.0 | ICD10 | Q89.0 Congenital malformations of spleen | UKB |
| Q89.1 | ICD10 | Q89.1 Congenital malformations of adrenal gland | UKB |
| Q89.2 | ICD10 | Q89.2 Congenital malformations of other endocrine glands | UKB |
| Q89.3 | ICD10 | Q89.3 Situs inversus | UKB |
| Q89.7 | ICD10 | Q89.7 Multiple congenital malformations, not elsewhere classified | UKB |
| Q89.8 | ICD10 | Q89.8 Other specified congenital malformations | UKB |
| 759 | ICD9 | 759 Other and unspecified congenital anomalies | UKB |
| 759.0 | ICD9 | 7590 Anomalies of spleen | UKB |
| 759.3 | ICD9 | 7593 Situs inversus | UKB |
| 759.4 | ICD9 | 7594 Conjoined twins | UKB |
| 759.5 | ICD9 | 7595 Tuberous sclerosis | UKB |
| 759.6 | ICD9 | 7596 Other hamartoses, not elsewhere classified | UKB |
| 759.7 | ICD9 | 7597 Multiple congenital anomalies, so described | UKB |
| 759.8 | ICD9 | 7598 Other specified anomalies | UKB |
| 759.89 | ICD9 | 75989 Other specified anomalies | UKB |
| 759.9 | ICD9 | 7599 Congenital anomaly, unspecified | UKB |
| 795.2 | ICD9 | 7952 Nonspecific abnormal findings on chromosomal analysis | UKB |
| V13.6 | ICD9 | V136 Personal history of congenital malformations | UKB |
This page is mainly a phenotype dictionary entry. When you are trying to find candidate PRS models, go to the Scores table, search by trait or exposure name, and then use the score-detail and PheWAS pages for model-specific follow-up.