multiple congenital anomalies-hypotonia-seizures syndrome 3
Human disease
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multiple congenital anomalies-hypotonia-seizures syndrome 3
Summary
multiple congenital anomalies-hypotonia-seizures syndrome 3 is a developmental defect during embryogenesis[1].
Key Facts
- multiple congenital anomalies-hypotonia-seizures syndrome 3's instance of is recorded as developmental defect during embryogenesis[2].
- multiple congenital anomalies-hypotonia-seizures syndrome 3's instance of is recorded as rare disease[3].
- multiple congenital anomalies-hypotonia-seizures syndrome 3's instance of is recorded as class of disease[4].
- multiple congenital anomalies-hypotonia-seizures syndrome 3 is a type of Slender bone dysplasia[5].
- multiple congenital anomalies-hypotonia-seizures syndrome 3 is a type of multiple congenital anomalies/dysmorphic syndrome-intellectual disability[6].
- multiple congenital anomalies-hypotonia-seizures syndrome 3 is a type of genetic syndromic intellectual disability[7].
- multiple congenital anomalies-hypotonia-seizures syndrome 3 is a type of multiple congenital anomalies-hypotonia-seizures syndrome[8].
- multiple congenital anomalies-hypotonia-seizures syndrome 3 is a type of autosomal recessive disease[9].
- multiple congenital anomalies-hypotonia-seizures syndrome 3's genetic association is recorded as PIGT[10].
- multiple congenital anomalies-hypotonia-seizures syndrome 3's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080140[11].
- multiple congenital anomalies-hypotonia-seizures syndrome 3's exact match is recorded as http://identifiers.org/doid/DOID:0080140[12].
- multiple congenital anomalies-hypotonia-seizures syndrome 3's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].