Retinal atrophy
Symptom Information:
Symptom ID: | HPO:0001105 | ||
Synonyms: |
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Quality: | |||
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) Abnormality of the globe(HPO:0012374) Abnormality of the posterior segment of the globe(HPO:0004329) Abnormality of the fundus(HPO:0001098) Abnormality of the retina(HPO:0000479) Retinal atrophy(HPO:0001105) MedDRA: |
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Database Frequency: | 10 / 7739 | ||
Resource: |
All diseases associated with this symptom:
CLN10 disease | (Orphanet:228337) |
Congenital neuronal ceroid lipofuscinosis | (Orphanet:168486) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 1 | (OMIM:236670) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 3 | (OMIM:253280) |
Muscle-eye-brain disease | (Orphanet:588) |
PORETTI-BOLTSHAUSER SYNDROME | (OMIM:615960) |
RETINITIS PIGMENTOSA 68 | (OMIM:615725) |
RETINOPATHY, PERICENTRAL PIGMENTARY, DOMINANT | (OMIM:180210) |
Retinitis pigmentosa 10 | (OMIM:180105) |
X-linked retinoschisis | (Orphanet:792) |