Long thin hands (rare)
Symptom Information:
Symptom ID: | OMIM : No Id available | ||
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Is a (Whole tree): |
HPO:
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Database Frequency: | 3 / 7739 | ||
Resource: |
All diseases associated with this symptom:
17q12 microdeletion syndrome | (Orphanet:261265) |
Intellectual deficit, X-linked, Snyder type | (Orphanet:3063) |
Oculocerebrofacial syndrome, Kaufman type | (Orphanet:2707) |