Related Conditions
Black locks, oculocutaneous albinism, AND deafness of the sensorineural type(child)
Tyrosinase-positive oculocutaneous albinism(child)
Tyrosinase-negative oculocutaneous albinism(child)
Oculocutaneous albinism type 4(child)
Microcephalus with albinism and digital anomaly syndrome(child)
Oculocutaneous albinism type 5(child)
Oculocutaneous albinism type 6(child)
Oculocutaneous albinism type 7(child)
Oculocutaneous albinism type 1(child)
Cross syndrome(child)
Oculocutaneous albinism type 8(child)
COMMAD (coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, deafness) syndrome(child)
Albinism(parent)
Hereditary disorder of the integument(parent)
Hereditary disorder of the visual system(parent)
Genetic disorder of skin pigmentation(parent)
Congenital oculocutaneous hypopigmentation(parent)
Recessive hereditary disorder (autosomal)(parent)
Quick Facts
- SNOMED CT
- 63844009
- UMLS CUI
- C0078918
- Fully Specified Name
- Oculocutaneous albinism (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.