Congenital disease
Disorder of connective tissue
|
|
Congenital connective tissue disorder (disorder)
Congenital connective tissue disorder
Id
363039000
Status
Defined
Finding site
Connective tissue structure
Occurrence
Congenital
SNOMED CT to ICD-10 extended map
Target
Q79.8
Rule
TRUE
Advice
ALWAYS Q79.8
Correlation
SNOMED CT source code to target map code correlation not specified
|
16q24.1 microdeletion syndrome
Allantoic cyst
Aneurysm osteoarthritis syndrome
Banki syndrome
Bilateral developmental anomaly of pleurae
Congenital absence of tendon
Congenital anomaly of cartilage
24
Congenital anomaly of peritoneum
11
Congenital anomaly of pleural folds
Congenital deformity of mitral valve annulus
Congenital epicardial cyst
Congenital Fanconi syndrome
Congenital generalized lipodystrophy
2
Congenital hypoplasia of annulus fibrosus of aorta
Congenital macular corneal dystrophy
1
Congenital malformation of vitreous humor
5
Congenital nephrotic syndrome, interstitial lung disease, epidermolysis bullosa syndrome
Congenital short costocoracoid ligament
Congenital shortening of tendon
2
Congenital stromal corneal dystrophy
Congenital syphilitic osteochondritis
Congenital trigger finger
2
Dilatation of tricuspid annulus
Ehlers-Danlos and osteogenesis imperfecta syndrome
Ehlers-Danlos syndrome
17
Extensor tendons of finger anomalies
Familial articular hypermobility syndrome
Farber's lipogranulomatosis
Hypoplasia of left atrioventricular valve annulus in double inlet ventricle
Hypoplasia of mitral valve annulus
Hypoplasia of right atrioventricular valve annulus in double inlet ventricle
Inherited cutis laxa
6
Late congenital syphilitic osteochondropathy
Leydig cell agenesis
2
Mandibuloacral dysostosis
2
Marfanoid habitus, inguinal hernia, advanced bone age syndrome
Neonatal Marfan syndrome
Progeroid and marfanoid aspect, lipodystrophy syndrome
Pulmonary valve ring hypoplasia
Severe myopia, generalized joint laxity, short stature syndrome
Tricuspid annulus hypoplasia
Williams syndrome
