Lisch nodules

Symptom Information:

Symptom ID: HPO:0009737
Synonyms:
Iris hamartomas [HPO:0009737]
Lisch nodules [OMIM:Lisch nodules]
Lisch nodules/iris hamartomas [Orphanet:4300]
Lisch nodules (iris hamartomas) [OMIM:Lisch nodules (iris hamartomas)]
Lisch nodules (iris hamartomas) (93%) [OMIM:Lisch nodules (iris hamartomas) (93%)]
Quality:
Cross references:
Orphanet:4300 "Lisch nodules/iris hamartomas" [Orphanet:4300]
OMIM: "Lisch nodules" [OMIM:Lisch nodules]
OMIM: "Lisch nodules (iris hamartomas)" [OMIM:Lisch nodules (iris hamartomas)]
OMIM: "Lisch nodules (iris hamartomas) (93%)" [OMIM:Lisch nodules (iris hamartomas) (93%)]
Is a (Direct Parents):
Orphanet Abnormality of the eye
HPO         Hamartoma of the eye
HPO         Abnormality of the iris
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the eye(HPO:0000478)
          Abnormal eye morphology(HPO:0012372)
             Hamartoma of the eye(HPO:0010568)
                Lisch nodules(HPO:0009737)
             Abnormality of the globe(HPO:0012374)
                Abnormality of the anterior segment of the globe(HPO:0004328)
                   Abnormality of the iris(HPO:0000525)
                      Lisch nodules(HPO:0009737)
                Abnormality of the uvea(HPO:0000553)
                   Abnormality of the iris(HPO:0000525)
                      Lisch nodules(HPO:0009737)
       Neoplasm(HPO:0002664)
          Neoplasm by histology(HPO:0011792)
             Hamartoma(HPO:0010566)
                Hamartoma of the eye(HPO:0010568)
                   Lisch nodules(HPO:0009737)
MedDRA:
Database Frequency: 10 / 7739
Resource:

All diseases associated with this symptom:

17q11 microdeletion syndrome (Orphanet:97685)
17q11.2 microduplication syndrome (Orphanet:139474)
NEUROFIBROMATOSIS, FAMILIAL SPINAL (OMIM:162210)
NEUROFIBROMATOSIS, TYPE III, MIXED CENTRAL AND PERIPHERAL (OMIM:162260)
NEUROFIBROMATOSIS, TYPE IV, OF RICCARDI (OMIM:162270)
Neurofibromatosis type 1 (Orphanet:636)
Neurofibromatosis type 1 due to NF1mutation or intragenic deletion (Orphanet:363700)
Neurofibromatosis type 6 (Orphanet:2678)
Watson syndrome (Orphanet:3444)
[DEL] NEUROFIBROMATOSIS-NOONAN SYNDROME (OMIM:601321)