Overview
Inherited arthrogryposis is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Familial arthrogryposis-cholestatic hepatorenal syndrome(child)
X-linked distal arthrogryposis multiplex congenita(child)
Van den Ende-Gupta syndrome(child)
Adducted thumbs and arthrogryposis syndrome Christian type(child)
Arthrogryposis multiplex congenita and whistling face syndrome(child)
Intellectual disability, developmental delay, contracture syndrome(child)
German syndrome(child)
X-linked lethal multiple pterygium syndrome(child)
Autosomal recessive myogenic arthrogryposis multiplex congenita(child)
Hypomyelination neuropathy arthrogryposis syndrome(child)
Hydrocephalus with cleft palate and joint contracture syndrome(child)
Freeman-Sheldon syndrome(child)
Malignant hyperthermia with arthrogryposis and torticollis syndrome(child)
Fetal akinesia, cerebral and retinal haemorrhage syndrome(child)
Contracture with ectodermal dysplasia and orofacial cleft syndrome(child)
Holoprosencephaly sequence with hypokinesia and congenital joint contracture syndrome(child)
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome(child)
Ehlers-Danlos syndrome musculocontractural type(child)
Congenital lethal myopathy Compton North type(child)
Lethal congenital contracture syndrome type 1(child)
Quick Facts
- SNOMED CT
- 28204005
- UMLS CUI
- C0265214
- Fully Specified Name
- Inherited arthrogryposis (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.