Premature separation of centromeric heterochromatin
Symptom Information:
Symptom ID: | HPO:0003616 | ||
Synonyms: |
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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 metabolism/homeostasis(HPO:0001939) Abnormality of cell physiology(HPO:0011017) Abnormality of chromosome segregation(HPO:0002916) Premature chromatid separation(HPO:0200024) Premature separation of centromeric heterochromatin(HPO:0003616) MedDRA: |
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Database Frequency: | 3 / 7739 | ||
Resource: |
All diseases associated with this symptom:
ROBERTS SYNDROME | (OMIM:268300) |
Roberts syndrome | (Orphanet:3103) |
SC PHOCOMELIA SYNDROME | (OMIM:269000) |