Osteogenesis imperfecta, recessive perinatal lethal, with microcephaly AND cataracts

disorder

SNOMED 15552004CUI C0268361

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Related Conditions

Congenital cataract(parent)

Hereditary disorder of the visual system(parent)

Osteogenesis imperfecta, perinatal lethal(parent)

Congenital microcephalus(parent)

Developmental hereditary disorder(parent)

Hereditary disorder of musculoskeletal system(parent)

Recessive hereditary disorder (autosomal)(parent)

Quick Facts

SNOMED CT: 15552004
UMLS CUI: C0268361
Fully Specified Name: Osteogenesis imperfecta, recessive perinatal lethal, with microcephaly AND cataracts (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.