Abnormality of brainstem morphology
Symptom Information:
Symptom ID: | HPO:0002363 | ||||||||
Synonyms: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
MedDRA: |
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Database Frequency: | 14 / 7739 | ||||||||
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All diseases associated with this symptom:
Alpha-N-acetylgalactosaminidase deficiency type 1 | (Orphanet:79279) |
Bosley-Salih-Alorainy syndrome | (Orphanet:69737) |
Cerebrotendinous xanthomatosis | (Orphanet:909) |
Christianson syndrome | (Orphanet:85278) |
Cobb syndrome | (Orphanet:53721) |
Fragile X-associated tremor/ataxia syndrome | (Orphanet:93256) |
Gómez-López-Hernández syndrome | (Orphanet:1532) |
Leber plus disease | (Orphanet:99718) |
Leukoencephalopathy - thalamus and brainstem anomalies - high lactate | (Orphanet:314051) |
MERRF | (Orphanet:551) |
Norrie disease | (Orphanet:649) |
Oculocerebral hypopigmentation syndrome, Preus type | (Orphanet:2720) |
PEHO syndrome | (Orphanet:2836) |
Progressive non-infectious anterior vertebral fusion | (Orphanet:2062) |