Abnormality of the diencephalon
Symptom Information:
Symptom ID: | HPO:0010662 | ||
Synonyms: |
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Is a (Whole tree): |
HPO:
MedDRA: |
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Database Frequency: | 6 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Holoprosencephaly - caudal dysgenesis | (Orphanet:2165) |
Morse-Rawnsley-Sargent syndrome | (Orphanet:2570) |
Norrie disease | (Orphanet:649) |
Oculocerebral hypopigmentation syndrome, Preus type | (Orphanet:2720) |
Rhombencephalosynapsis | (Orphanet:59315) |
Williams syndrome | (Orphanet:904) |