Lisch nodules
Symptom Information:
Symptom ID: | HPO:0009737 | ||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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: |
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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) |