Abnormality of prenatal development or birth
Symptom Information:
Symptom ID: | HPO:0001197 | ||
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 prenatal development or birth(HPO:0001197) MedDRA: |
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Database Frequency: | 9 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Axial mesodermal dysplasia spectrum | (Orphanet:1834) |
Congenital pulmonary airway malformation | (Orphanet:2444) |
Diffuse neonatal hemangiomatosis | (Orphanet:2123) |
Distal monosomy 17q | (Orphanet:1597) |
Gestational trophoblastic neoplasm | (Orphanet:59305) |
Hydatidiform mole | (Orphanet:99927) |
Maternal hyperphenylalaninemia | (Orphanet:2209) |
Maternal hyperthermia induced birth defects | (Orphanet:2216) |
Placental site trophoblastic tumor | (Orphanet:99928) |