Overview
X-linked recessive hereditary disease is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Syndromic X-linked intellectual disability due to jumonji at-rich interactive domain 1c mutation(child)
Pallister W syndrome(child)
X-linked recessive sensory neuropathy(child)
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Chondrodysplasia punctata, X-linked recessive type(child)
X-linked recessive intellectual disability and macrocephaly with ciliary dysfunction syndrome(child)
X-linked intellectual disability with seizure and psoriasis syndrome(child)
Bornholm eye disease(child)
Sengers Hamel Otten syndrome(child)
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X-linked intellectual disability with ataxia and apraxia syndrome(child)
Chromosome Xp11.3 microdeletion syndrome(child)
SCARF (skeletal abnormality, cutis laxa, craniostenosis, ambiguous genitalia, retardation, facial abnormality) syndrome(child)
X-linked intellectual disability with cubitus valgus and dysmorphism syndrome(child)
Microphthalmia with ankyloblepharon and intellectual disability syndrome(child)
X-linked epilepsy with learning disability and behavior disorder syndrome(child)
X-linked intellectual disability Shrimpton type(child)
X-linked intellectual disability Pai type(child)
N syndrome(child)
X-linked spasticity, intellectual disability, epilepsy syndrome(child)
Quick Facts
- SNOMED CT
- 1162976004
- UMLS CUI
- C5566660
- Fully Specified Name
- X-linked recessive hereditary disease (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.