Overview
Heterochromic iris 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.
Fuchs' heterochromic cyclitis
Frequent (30-79%)
Sturge-Weber sequence
Occasional (5-29%)
Tyrosinase-positive oculocutaneous albinism
Frequent (30-79%)
Familial dysautonomia
Occasional (5-29%)
Waardenburg's syndrome
Very frequent (80-99%)
Neurofibromatosis type 1
Frequent (30-79%)
Facial hemiatrophy
Occasional (5-29%)
Iridocorneal endothelial syndrome
Very rare (1-4%)
Klein-Waardenberg's syndrome
Woolly hair naevus
Occasional (5-29%)
Retinoblastoma
Occasional (5-29%)
Albinism-deafness syndrome of Tietz
Excluded (<1%)
Posterior fossa brain malformation, haemangioma, arterial anomaly, cardiac defect and aortic coarctation, and eye abnormality syndrome
Occasional (5-29%)
Waardenburg syndrome co-occurrent with Hirschsprung disease
Proteus like syndrome
Frequent (30-79%)
Piebaldism
Occasional (5-29%)
Progressive hemifacial atrophy
Occasional (5-29%)
Deafness and hypogonadism syndrome
Occasional (5-29%)
Albinism with deafness syndrome
Occasional (5-29%)
Sensorineural hearing loss, early graying, essential tremor syndrome
Occasional (5-29%)
Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease
Very frequent (80-99%)
Trisomy 8p syndrome
Frequent (30-79%)
Congenital Horner syndrome
Piebald trait with neurologic defects syndrome
Occasional (5-29%)
Waardenburg syndrome type 1
Very frequent (80-99%)
Quick Facts
- SNOMED CT
- 247033008
- UMLS CUI
- C0423318
- Fully Specified Name
- Heterochromic iris (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.