Blue irides

Symptom Information:

Symptom ID: HPO:0000635
Synonyms:
Blue eyes [HPO:0000635]
Blue eyes [OMIM:Blue eyes]
Blue irides [OMIM:Blue irides]
Blue eyes (Japanese patients) [OMIM:Blue eyes (Japanese patients)]
Quality:
Cross references:
OMIM: "Blue eyes" [OMIM:Blue eyes]
OMIM: "Blue irides" [OMIM:Blue irides]
OMIM: "Blue eyes (Japanese patients)" [OMIM:Blue eyes (Japanese patients)]
Is a (Direct Parents):
HPO         Abnormal iris pigmentation
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the eye(HPO:0000478)
          Abnormal eye morphology(HPO:0012372)
             Abnormality of the globe(HPO:0012374)
                Abnormality of the anterior segment of the globe(HPO:0004328)
                   Abnormality of the iris(HPO:0000525)
                      Abnormal iris pigmentation(HPO:0008034)
                         Blue irides(HPO:0000635)
                Abnormality of the uvea(HPO:0000553)
                   Abnormality of the iris(HPO:0000525)
                      Abnormal iris pigmentation(HPO:0008034)
                         Blue irides(HPO:0000635)
MedDRA:
Database Frequency: 25 / 7739
Resource:

All diseases associated with this symptom:

ACRODYSOSTOSIS 1 WITH OR WITHOUT HORMONE RESISTANCE (OMIM:101800)
ACRODYSOSTOSIS 2 WITH OR WITHOUT HORMONE RESISTANCE (OMIM:614613)
Acrodysostosis with multiple hormone resistance (Orphanet:280651)
Angelman syndrome (Orphanet:72)
Developmental delay with autism spectrum disorder and gait instability (Orphanet:329195)
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1 (OMIM:129900)
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME3 (OMIM:604292)
EEC syndrome (Orphanet:1896)
METHIONINE MALABSORPTION SYNDROME (OMIM:250900)
Maternal hyperphenylalaninemia (Orphanet:2209)
Minimal pigment oculocutaneous albinism type 1 (Orphanet:352734)
NOONAN SYNDROME 4 (OMIM:610733)
Oculocutaneous albinism type 1 (Orphanet:352731)
Oculocutaneous albinism type 2 (Orphanet:79432)
Oculocutaneous albinism type 4 (Orphanet:79435)
Phenylketonuria (Orphanet:716)
SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 11 (OMIM:612271)
Tietz syndrome (Orphanet:42665)
Urocanic aciduria (Orphanet:210128)
WAARDENBURG SYNDROME, TYPE 2E (OMIM:611584)
WAARDENBURG SYNDROME, TYPE 4B (OMIM:613265)
WAARDENBURG SYNDROME, TYPE 4C (OMIM:613266)
Waardenburg syndrome (Orphanet:3440)
Waardenburg-Shah syndrome (Orphanet:897)
Williams syndrome (Orphanet:904)