TARP syndrome
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TARP syndrome
Summary
TARP syndrome is a head and neck disease[1].
Key Facts
- TARP syndrome's instance of is recorded as head and neck disease[2].
- TARP syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- TARP syndrome's instance of is recorded as rare disease[4].
- TARP syndrome's instance of is recorded as class of disease[5].
- TARP syndrome is a type of genetic syndromic Pierre robin syndrome[6].
- TARP syndrome is a type of rare syndrome with cardiac malformations[7].
- TARP syndrome is a type of syndrome[8].
- TARP syndrome is a type of X-linked disease[9].
- TARP syndrome's symptoms and signs is recorded as micrognathism[10].
- TARP syndrome's symptoms and signs is recorded as isolated cleft palate[11].
- TARP syndrome's symptoms and signs is recorded as clubfoot[12].
- TARP syndrome's symptoms and signs is recorded as atrial heart septal defect[13].
- TARP syndrome's symptoms and signs is recorded as persistent left superior vena cava[14].
- TARP syndrome's genetic association is recorded as RBM10[15].
- TARP syndrome's age of onset is recorded as congenital onset[16].
- TARP syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2886[17].
- TARP syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111780[18].
- TARP syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0111780[19].