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]. It draws 33 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #103 of 308).[2]
Key Facts
- Cantú syndrome's image is recorded as Photo-of-the-person-with-cantu-syndrome.gif[3].
- Cantú syndrome's instance of is recorded as developmental defect during embryogenesis[4].
- Cantú syndrome's instance of is recorded as rare disease[5].
- Cantú syndrome's instance of is recorded as class of disease[6].
- Cantú syndrome's subclass of is recorded as osteochondrodysplasia[7].
- Cantú syndrome's subclass of is recorded as hypertrichosis[8].
- Cantú syndrome's subclass of is recorded as cardiomegaly[9].
- Cantú syndrome's subclass of is recorded as dysostosis with predominant craniofacial involvement[10].
- Cantú syndrome's subclass of is recorded as multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome[11].
- Cantú syndrome's Commons category is recorded as Cantú syndrome[12].
- Cantú syndrome's MeSH descriptor ID is recorded as C535572[13].
- Cantú syndrome's OMIM ID is recorded as 239850[14].
- Cantú syndrome's DiseasesDB is recorded as 34853[15].
- Cantú syndrome's Disease Ontology ID is recorded as DOID:0060569[16].
- Cantú syndrome's symptoms and signs is recorded as hypertrichosis[17].
- Cantú syndrome's Orphanet ID is recorded as 1517[18].
- Cantú syndrome's genetic association is recorded as ABCC9[19].
- Cantú syndrome's genetic association is recorded as KCNJ8[20].
- Cantú syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060569[21].
- Cantú syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060569[22].
- Cantú syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1517[23].
- Cantú syndrome's UMLS CUI is recorded as C0795905[24].
- Cantú syndrome's ICD-10-CM is recorded as Q87.3[25].
- Cantú syndrome's GARD rare disease ID is recorded as 8585[26].
- Cantú syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[27].
Why It Matters
Cantú syndrome draws 33 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #103 of 308).[2]