Increased nuchal translucency
Symptom Information:
Symptom ID: | HPO:0010880 | ||||||
Synonyms: |
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Quality: | |||||||
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) Increased nuchal translucency(HPO:0010880) Abnormality of metabolism/homeostasis(HPO:0001939) Abnormality of fluid regulation(HPO:0011032) Edema(HPO:0000969) Increased nuchal translucency(HPO:0010880) MedDRA: |
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Database Frequency: | 13 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
Auriculoocular anomalies - cleft lip | (Orphanet:71270) |
Autosomal recessive omodysplasia | (Orphanet:93329) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Cornelia de Lange syndrome | (Orphanet:199) |
Diaphanospondylodysostosis | (Orphanet:66637) |
Fetal parvovirus syndrome | (Orphanet:295) |
Mosaic variegated aneuploidy syndrome | (Orphanet:1052) |
Smith-Lemli-Opitz syndrome | (Orphanet:818) |
Thanatophoric dysplasia | (Orphanet:2655) |
Thanatophoric dysplasia type 1 | (Orphanet:1860) |
Thanatophoric dysplasia type 2 | (Orphanet:93274) |
Trisomy 1q | (Orphanet:261344) |
Williams syndrome | (Orphanet:904) |