Embryofetopathy due to oral anticoagulant therapy

General Information (adopted from Orphanet):

Synonyms, Signs: Vitamin K antagonists embryofetopathy
Coumarin embryopathy
Fetal warfarin syndrome
Number of Symptoms 27
OrphanetNr: 1914
OMIM Id:
ICD-10: Q86.2
UMLs:
MeSH:
MedDRA:
Snomed:

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: Sort by abundance 

1
(HPO:0000470) Short neck Frequent [Orphanet] 345 / 7739
2
(HPO:0000463) Anteverted nares Very frequent [Orphanet] 305 / 7739
3
(HPO:0005280) Depressed nasal bridge Very frequent [Orphanet] 381 / 7739
4
(HPO:0003196) Short nose Very frequent [Orphanet] 264 / 7739
5
(HPO:0000316) Hypertelorism Occasional [Orphanet] 644 / 7739
6
(HPO:0000158) Macroglossia Occasional [Orphanet] 119 / 7739
7
(HPO:0000453) Choanal atresia Occasional [Orphanet] 76 / 7739
8
(HPO:0000520) Proptosis Occasional [Orphanet] 192 / 7739
9
(HPO:0008056) Aplasia/Hypoplasia affecting the eye Occasional [Orphanet] 142 / 7739
10
(HPO:0000518) Cataract Occasional [Orphanet] 454 / 7739
11
(HPO:0000572) Visual loss Occasional [Orphanet] 272 / 7739
12
(HPO:0008772) Aplasia/Hypoplasia of the external ear Occasional [Orphanet] 67 / 7739
13
(HPO:0000365) Hearing impairment Occasional [Orphanet] 539 / 7739
14
(HPO:0001250) Seizures Occasional [Orphanet] 1245 / 7739
15
(HPO:0010655) Epiphyseal stippling Very frequent [Orphanet] 32 / 7739
16
(HPO:0002475) Myelomeningocele Occasional [Orphanet] 29 / 7739
17
(HPO:0009882) Short distal phalanx of finger Frequent [Orphanet] 125 / 7739
18
(HPO:0004279) Short palm Frequent [Orphanet] 323 / 7739
19
(HPO:0003468) Abnormality of the vertebrae Very frequent [Orphanet] 77 / 7739
20
(HPO:0001511) Intrauterine growth retardation Frequent [Orphanet] 358 / 7739
21
(HPO:0001804) Hypoplastic fingernail Frequent [Orphanet] 62 / 7739
22
(HPO:0030680) Abnormality of cardiovascular system morphology Occasional [Orphanet] 355 / 7739
23
(HPO:0002093) Respiratory insufficiency Frequent [Orphanet] 410 / 7739
24
(HPO:0001252) Muscular hypotonia Occasional [Orphanet] 990 / 7739
25
(HPO:0012758) Neurodevelopmental delay Frequent [Orphanet] 949 / 7739
26
(HPO:0000238) Hydrocephalus Occasional [Orphanet] 278 / 7739
27
(HPO:0012795) Abnormality of the optic disc Occasional [Orphanet] 187 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: