syndromic X-linked intellectual disability Claes-Jensen type
Human disease
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syndromic X-linked intellectual disability Claes-Jensen type
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's subclass of is recorded as X-linked intellectual disability[5].
- syndromic X-linked intellectual disability Claes-Jensen type's subclass of is recorded as multiple congenital anomalies/dysmorphic syndrome-intellectual disability[6].
- syndromic X-linked intellectual disability Claes-Jensen type's subclass of is recorded as monogenic disease with epilepsy[7].
- syndromic X-linked intellectual disability Claes-Jensen type's subclass of is recorded as X-linked recessive disease[8].
- syndromic X-linked intellectual disability Claes-Jensen type's MeSH descriptor ID is recorded as C564494[9].
- syndromic X-linked intellectual disability Claes-Jensen type's OMIM ID is recorded as 300534[10].
- syndromic X-linked intellectual disability Claes-Jensen type's Disease Ontology ID is recorded as DOID:0060809[11].
- syndromic X-linked intellectual disability Claes-Jensen type's Orphanet ID is recorded as 85279[12].
- syndromic X-linked intellectual disability Claes-Jensen type's health specialty is recorded as medical genetics[13].
- syndromic X-linked intellectual disability Claes-Jensen type's genetic association is recorded as KDM5C[14].
- syndromic X-linked intellectual disability Claes-Jensen type's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060809[15].
- syndromic X-linked intellectual disability Claes-Jensen type's exact match is recorded as http://identifiers.org/doid/DOID:0060809[16].
- syndromic X-linked intellectual disability Claes-Jensen type's UMLS CUI is recorded as C1845243[17].
- syndromic X-linked intellectual disability Claes-Jensen type's UMLS CUI is recorded as C5681493[18].
- syndromic X-linked intellectual disability Claes-Jensen type's ICD-10-CM is recorded as Q87.8[19].
- syndromic X-linked intellectual disability Claes-Jensen type's on focus list of Wikimedia project is recorded as WikiProject Medicine[20].
- syndromic X-linked intellectual disability Claes-Jensen type's Mondo ID is recorded as MONDO_0010355[21].
- syndromic X-linked intellectual disability Claes-Jensen type's UniProt disease ID is recorded as DI-00718[22].