Disorder of connective tissue
Hereditary disease
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Connective tissue hereditary disorder (disorder)
Connective tissue hereditary disorder
Inherited disorder of connective tissue
hereditaire aandoening van bindweefsel
erfelijke bindweefselaandoening
Id363045008
StatusDefined
Finding siteConnective tissue structure
ICD-10 complex map reference set
Target
RuleTRUE
AdviceMAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA
CorrelationSNOMED CT source code to target map code correlation not specified
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AKT2-related familial partial lipodystrophy
Aneurysm osteoarthritis syndrome
Autoimmune interstitial lung disease, arthritis syndrome
Autosomal dominant neovascular inflammatory vitreoretinopathy
Autosomal semi-dominant severe lipodystrophic laminopathy
Autosomal systemic lupus erythematosus
Banki syndrome
Blindness, scoliosis, arachnodactyly syndrome
Carpotarsal osteochondromatosis
Chronic respiratory distress with surfactant metabolism deficiency
CIDEC-related familial partial lipodystrophy
Congenital nephrotic syndrome, interstitial lung disease, epidermolysis bullosa syndrome
Congenital short costocoracoid ligament
Congenital stromal corneal dystrophy
Dysplasia epiphysealis hemimelica
Ehlers-Danlos syndrome19
Exostosis, anetoderma, brachydactyly type E syndrome
Extensor tendons of finger anomalies
Familial chondromalacia of patella
Familial interstitial nephritis
Familial partial lipodystrophy Dunnigan type
Familial partial lipodystrophy Dunnigan type
Familial partial lipodystrophy Kobberling type
Familial partial lipodystrophy Kobberling type
Farber's lipogranulomatosis
Fleck corneal dystrophy
Gelatinous droplike corneal dystrophy
Generalized congenital lipodystrophy with myopathy
Genochondromatosis type 1
Genochondromatosis type 2
Gitelman syndrome
Gnathodiaphyseal dysplasia
Goldmann-Favre syndrome
Grange syndrome
Granular corneal dystrophy2
Hereditary fibrosing poikiloderma, tendon contractures, myopathy, pulmonary fibrosis syndrome
Hereditary lipodystrophy
Hereditary tubulointerstitial disorder
Hereditary vitreoretinopathy3
Hypermobility syndrome4
Hypoplasia and coloboma of alar cartilage with telecanthus syndrome
Infantile nephropathic cystinosis1
Inherited cutis laxa8
Inherited pseudoxanthoma elasticum2
Interstitial lung disease due to ABCA3 deficiency
Interstitial lung disease due to surfactant protein C deficiency
Karyomegalic interstitial nephritis
Keppen Lubinsky syndrome
Keutel syndrome
Lattice corneal dystrophy2
Leydig cell agenesis3
LIPE-related familial partial lipodystrophy
Lipodystrophy, intellectual disability, deafness syndrome
Macular corneal dystrophy5
Mandibuloacral dysostosis2
Marden Walker syndrome
Marfan's syndrome8
Metachondromatosis
Metaphyseal chondrodysplasia, McKusick type
Metaphyseal chondromatosis co-occurrent with D-2 hydroxyglutaric aciduria
Multiple congenital exostosis15
Nephropathic cystinosis
Perilipin 1 related familial partial lipodystrophy
Perilipin 1 related familial partial lipodystrophy
Posterior amorphous corneal dystrophy
PPARG-related familial partial lipodystrophy
Pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome
Pulmonary interstitial glycogenosis
Retinal detachment and occipital encephalocele
Schnyder crystalline cornea dystrophy
Severe early-onset pulmonary alveolar proteinosis due to MARS deficiency
Severe myopia, generalized joint laxity, short stature syndrome
Severe neurodegenerative syndrome with lipodystrophy
Severe neurodegenerative syndrome with lipodystrophy
Shell teeth
Shprintzen Goldberg craniosynostosis syndrome
Spondyloenchondromatosis1
Spondyloepimetaphyseal dysplasia, short limb, abnormal calcification syndrome
Upington disease