RxDB
ICD-9-CM Codes ICD-9-PCS Codes

759.89 - Other specified congenital anomalies

Overview

GEM Conversion to ICD-10 CM

Fs: 10000 – Barth syndrome
Fs: 10000 – Smith-Lemli-Opitz syndrome
Fs: 10000 – Congenital malformation syndromes predominantly involving limbs
Fs: 10000 – Congenital malformation syndromes involving early overgrowth
Fs: 10000 – Other congenital malformation syndromes with other skeletal changes
Fs: 10000 – Alport syndrome
Fs: 10000 – Arterial tortuosity syndrome
Fs: 10000 – Other specified congenital malformation syndromes, not elsewhere classified
Fs: 10000 – Other specified congenital malformations

Sibling Codes

Prader-Willi syndrome
Marfan syndrome
Fragile X syndrome
Other specified congenital anomalies

Parent Sibling Codes

Anomalies of spleen
Anomalies of adrenal gland
Anomalies of other endocrine glands
Situs inversus
Conjoined twins
Tuberous sclerosis
Other hamartoses, not elsewhere classified
Multiple congenital anomalies, so described
Congenital anomaly, unspecified