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's subclass of is recorded as genetic syndromic Pierre robin syndrome[6].
- TARP syndrome's subclass of is recorded as rare syndrome with cardiac malformations[7].
- TARP syndrome's subclass of is recorded as syndrome[8].
- TARP syndrome's subclass of is recorded as X-linked disease[9].
- TARP syndrome's MeSH descriptor ID is recorded as C536942[10].
- TARP syndrome's OMIM ID is recorded as 311900[11].
- TARP syndrome's KEGG ID is recorded as H00943[12].
- TARP syndrome's Disease Ontology ID is recorded as DOID:0111780[13].
- TARP syndrome's symptoms and signs is recorded as micrognathism[14].
- TARP syndrome's symptoms and signs is recorded as isolated cleft palate[15].
- TARP syndrome's symptoms and signs is recorded as clubfoot[16].
- TARP syndrome's symptoms and signs is recorded as atrial heart septal defect[17].
- TARP syndrome's symptoms and signs is recorded as persistent left superior vena cava[18].
- TARP syndrome's Orphanet ID is recorded as 2886[19].
- TARP syndrome's genetic association is recorded as RBM10[20].
- TARP syndrome's Google Knowledge Graph ID is recorded as /g/11qplpvlt2[21].
- TARP syndrome's age of onset is recorded as congenital onset[22].
- TARP syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2886[23].
- TARP syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111780[24].
- TARP syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0111780[25].
- TARP syndrome's UMLS CUI is recorded as C1839463[26].