syndromic X-linked intellectual disability Raymond type
syndromic X-linked intellectual disability characterized by intellectual disability and marfanoid habitus that has material basis in mutation in the ZDHHC9 gene on chromosome Xq26.1
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Summary
syndromic X-linked intellectual disability Raymond type is a rare disease[1].
Key Facts
- syndromic X-linked intellectual disability Raymond type's instance of is recorded as rare disease[2].
- syndromic X-linked intellectual disability Raymond type's instance of is recorded as class of disease[3].
- syndromic X-linked intellectual disability Raymond type's subclass of is recorded as X-linked intellectual disability[4].
- syndromic X-linked intellectual disability Raymond type's OMIM ID is recorded as 300799[5].
- syndromic X-linked intellectual disability Raymond type's Disease Ontology ID is recorded as DOID:0060824[6].
- syndromic X-linked intellectual disability Raymond type's Orphanet ID is recorded as 163953[7].
- syndromic X-linked intellectual disability Raymond type's health specialty is recorded as medical genetics[8].
- syndromic X-linked intellectual disability Raymond type's genetic association is recorded as ZDHHC9[9].
- syndromic X-linked intellectual disability Raymond type's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060824[10].
- syndromic X-linked intellectual disability Raymond type's exact match is recorded as http://identifiers.org/doid/DOID:0060824[11].
- syndromic X-linked intellectual disability Raymond type's UMLS CUI is recorded as C3275406[12].
- syndromic X-linked intellectual disability Raymond type's UMLS CUI is recorded as C2749033[13].
- syndromic X-linked intellectual disability Raymond type's ICD-10-CM is recorded as Alexandria.8[14].
- syndromic X-linked intellectual disability Raymond type's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- syndromic X-linked intellectual disability Raymond type's Mondo ID is recorded as MONDO_0010427[16].
- syndromic X-linked intellectual disability Raymond type's UniProt disease ID is recorded as DI-02508[17].