syndromic X-linked intellectual disability Claes-Jensen type
Human disease
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Summary
syndromic X-linked intellectual disability Claes-Jensen type is a developmental defect during embryogenesis[1].
Key Facts
- syndromic X-linked intellectual disability Claes-Jensen type's instance of is recorded as developmental defect during embryogenesis[2].
- syndromic X-linked intellectual disability Claes-Jensen type's instance of is recorded as rare disease[3].
- syndromic X-linked intellectual disability Claes-Jensen type's instance of is recorded as class of disease[4].
- syndromic X-linked intellectual disability Claes-Jensen type is a type of X-linked intellectual disability[5].
- syndromic X-linked intellectual disability Claes-Jensen type is a type of multiple congenital anomalies/dysmorphic syndrome-intellectual disability[6].
- syndromic X-linked intellectual disability Claes-Jensen type is a type of monogenic disease with epilepsy[7].
- syndromic X-linked intellectual disability Claes-Jensen type is a type of X-linked recessive disease[8].
- syndromic X-linked intellectual disability Claes-Jensen type's health specialty is recorded as medical genetics[9].
- syndromic X-linked intellectual disability Claes-Jensen type's genetic association is recorded as KDM5C[10].
- syndromic X-linked intellectual disability Claes-Jensen type's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060809[11].
- syndromic X-linked intellectual disability Claes-Jensen type's exact match is recorded as http://identifiers.org/doid/DOID:0060809[12].
- syndromic X-linked intellectual disability Claes-Jensen type's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].