Cocaine embryofetopathy
General Information (adopted from Orphanet):
| Synonyms, Signs: |
Fetal cocaine syndrome |
| Number of Symptoms | 8 |
| OrphanetNr: | 1911 |
| OMIM Id: |
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| ICD-10: |
Q86.8 |
| UMLs: |
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| MeSH: |
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| MedDRA: |
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| Snomed: |
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Prevalence, inheritance and age of onset:
| Prevalence: | No data available. |
| Inheritance: |
Not applicable [Orphanet] |
| Age of onset: |
Antenatal Neonatal [Orphanet] |
Disease classification (adopted from Orphanet):
| Parent Diseases: |
Teratogenic Pierre Robin syndrome
-Rare developmental defect during embryogenesis -Rare genetic disease -Rare maxillo-facial surgical disease -Rare otorhinolaryngologic disease Toxic or drug-related embryofetopathy -Rare developmental defect during embryogenesis |
Symptom Information:
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(HPO:0000079) | Abnormality of the urinary system | Occasional [Orphanet] | 88 / 7739 | |||
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(HPO:0002084) | Encephalocele | Occasional [Orphanet] | 70 / 7739 | |||
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(HPO:0001347) | Hyperreflexia | Very frequent [Orphanet] | 363 / 7739 | |||
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(HPO:0001276) | Hypertonia | Very frequent [Orphanet] | 317 / 7739 | |||
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(HPO:0009882) | Short distal phalanx of finger | Occasional [Orphanet] | 125 / 7739 | |||
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(HPO:0100657) | Thoracoabdominal eventration | Occasional [Orphanet] | 2 / 7739 | |||
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(HPO:0002242) | Abnormality of the intestine | Occasional [Orphanet] | 42 / 7739 | |||
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(HPO:0001626) | Abnormality of the cardiovascular system | Occasional [Orphanet] | 73 / 7739 |
Associated genes:
ClinVar (via SNiPA)
| Gene symbol | Variation | Clinical significance | Reference |
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