Overview
Iris hypopigmentation is a finding that may indicate an underlying health condition requiring clinical evaluation.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Tyrosinase-negative oculocutaneous albinism
Very frequent (80-99%)
Hermansky-Pudlak syndrome
Very frequent (80-99%)
Cross syndrome
Occasional (5-29%)
Tyrosinase-positive oculocutaneous albinism
Frequent (30-79%)
Hypopigmentation-immunodeficiency disease
Occasional (5-29%)
Rufous albinism
Frequent (30-79%)
Angelman syndrome
Frequent (30-79%)
X-linked ocular albinism, Nettleship type
Very frequent (80-99%)
Yellow mutant oculocutaneous albinism
Very frequent (80-99%)
Chediak-Higashi syndrome
Frequent (30-79%)
Adult vitelliform macular dystrophy
Frequent (30-79%)
Usher syndrome type 2
Very frequent (80-99%)
3-Methylglutaconic aciduria type 4
Occasional (5-29%)
Congenital miosis
Very frequent (80-99%)
Progressive bulbar palsy with sensorineural deafness
Occasional (5-29%)
Oculocutaneous albinism type 4
Frequent (30-79%)
Spondyloocular syndrome
Very frequent (80-99%)
Oculocerebral hypopigmentation syndrome of Preus type
Very frequent (80-99%)
Koolen De Vries syndrome
Frequent (30-79%)
8q21.11 microdeletion syndrome
Occasional (5-29%)
Microcephalus with albinism and digital anomaly syndrome
Very frequent (80-99%)
Chromosome Xp11.3 microdeletion syndrome
Very frequent (80-99%)
Deaf blind hypopigmentation syndrome Yemenite type
Frequent (30-79%)
Oculocutaneous albinism type 1
Very frequent (80-99%)
Usher syndrome type 3
Very frequent (80-99%)
Quick Facts
- SNOMED CT
- 247032003
- UMLS CUI
- C0154920
- Fully Specified Name
- Iris hypopigmentation (finding)
- Associated Conditions
- 25
- Diagnostic Tests
- 0
This information is for educational purposes only. If you are experiencing symptoms, please consult a healthcare provider for proper evaluation and diagnosis.