heart defect-tongue hamartoma-polysyndactyly syndrome
human disease
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heart defect-tongue hamartoma-polysyndactyly syndrome
Summary
heart defect-tongue hamartoma-polysyndactyly syndrome is a developmental defect during embryogenesis[1].
Key Facts
- heart defect-tongue hamartoma-polysyndactyly syndrome's instance of is recorded as developmental defect during embryogenesis[2].
- heart defect-tongue hamartoma-polysyndactyly syndrome's instance of is recorded as rare disease[3].
- heart defect-tongue hamartoma-polysyndactyly syndrome's instance of is recorded as class of disease[4].
- heart defect-tongue hamartoma-polysyndactyly syndrome is a type of multiple congenital anomalies/dysmorphic syndrome without intellectual disability[5].
- heart defect-tongue hamartoma-polysyndactyly syndrome is a type of rare genetic developmental defect during embryogenesis[6].
- heart defect-tongue hamartoma-polysyndactyly syndrome is a type of autosomal recessive disease[7].
- heart defect-tongue hamartoma-polysyndactyly syndrome is a type of syndrome[8].
- heart defect-tongue hamartoma-polysyndactyly syndrome's genetic association is recorded as WDPCP[9].
- heart defect-tongue hamartoma-polysyndactyly syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1338[10].
- heart defect-tongue hamartoma-polysyndactyly syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111591[11].
- heart defect-tongue hamartoma-polysyndactyly syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0111591[12].