Cantú syndrome
osteochondrodysplasia characterized by congenital hypertrichosis, neonatal macrosomia, and cardiomegaly
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Cantú syndrome
Summary
Cantú syndrome is a developmental defect during embryogenesis[1].
Key Facts
- Cantú syndrome's instance of is recorded as developmental defect during embryogenesis[2].
- Cantú syndrome's instance of is recorded as rare disease[3].
- Cantú syndrome's instance of is recorded as class of disease[4].
- Cantú syndrome is a type of osteochondrodysplasia[5].
- Cantú syndrome is a type of hypertrichosis[6].
- Cantú syndrome is a type of cardiomegaly[7].
- Cantú syndrome is a type of dysostosis with predominant craniofacial involvement[8].
- Cantú syndrome is a type of multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome[9].
- Cantú syndrome's Commons category is recorded as Cantú syndrome[10].
- Cantú syndrome's symptoms and signs is recorded as hypertrichosis[11].
- Cantú syndrome's genetic association is recorded as ABCC9[12].
- Cantú syndrome's genetic association is recorded as KCNJ8[13].
- Cantú syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060569[14].
- Cantú syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060569[15].
- Cantú syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1517[16].
- Cantú syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[17].