Normal karyotype
Symptom Information:
Symptom ID: | OMIM : No Id available | |
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Is a (Whole tree): |
HPO:
MedDRA: |
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Database Frequency: | 5 / 7739 | |
Resource: |
All diseases associated with this symptom:
Cervicofacial lymphatic malformation | (Orphanet:137923) |
Cystic hygroma | (Orphanet:79486) |
Holoprosencephaly - postaxial polydactyly | (Orphanet:2166) |
ROBERTS SYNDROME | (OMIM:268300) |
Radio-ulnar synostosis - amegakaryocytic thrombocytopenia | (Orphanet:71289) |