branchioskeletogenital syndrome
human disease
Press Enter · cited answer in seconds
0 sources
Summary
branchioskeletogenital syndrome is a developmental defect during embryogenesis[1]. It is known by 7 alternative names across languages and contexts.[2]
Key Facts
- branchioskeletogenital syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- branchioskeletogenital syndrome's instance of is recorded as class of disease[4].
- branchioskeletogenital syndrome is a type of genetic syndromic intellectual disability[5].
- branchioskeletogenital syndrome is a type of multiple congenital anomalies/dysmorphic syndrome-intellectual disability[6].
- branchioskeletogenital syndrome is a type of syndromic urogenital tract malformation[7].
- branchioskeletogenital syndrome is a type of syndrome[8].
- branchioskeletogenital syndrome's symptoms and signs is recorded as ptosis[9].
- branchioskeletogenital syndrome's genetic association is recorded as CDH11[10].
- branchioskeletogenital syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1299[11].
- branchioskeletogenital syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080631[12].
- branchioskeletogenital syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0080631[13].
Why It Matters
branchioskeletogenital syndrome is known by 7 alternative names across languages and contexts.[2]