Abnormality of chromosome segregation
Symptom Information:
Symptom ID: | HPO:0002916 | ||
Synonyms: |
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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 metabolism/homeostasis(HPO:0001939) Abnormality of cell physiology(HPO:0011017) Abnormality of chromosome segregation(HPO:0002916) MedDRA: |
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Database Frequency: | 5 / 7739 | ||
Resource: |
All diseases associated with this symptom:
FRAGILE SITE, DISTAMYCIN A TYPE, RARE, FRA(16)(q22.1) | (OMIM:136580) |
Hypoplastic left heart syndrome | (Orphanet:2248) |
NONDISJUNCTION | (OMIM:158250) |
PELGER-HUET ANOMALY | (OMIM:169400) |
Solitary median maxillary central incisor syndrome | (Orphanet:2286) |