autism, susceptibility to, X-linked 4
human disease
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autism, susceptibility to, X-linked 4
Summary
autism, susceptibility to, X-linked 4 is a class of disease[1].
Key Facts
- autism, susceptibility to, X-linked 4's instance of is recorded as class of disease[2].
- autism, susceptibility to, X-linked 4's subclass of is recorded as partial monosomy of the short arm of chromosome X[3].
- autism, susceptibility to, X-linked 4's subclass of is recorded as heritability of autism[4].
- autism, susceptibility to, X-linked 4's OMIM ID is recorded as 300830[5].
- autism, susceptibility to, X-linked 4's Orphanet ID is recorded as 106[6].
- autism, susceptibility to, X-linked 4's genetic association is recorded as PTCHD1[7].
- autism, susceptibility to, X-linked 4's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_106[8].
- autism, susceptibility to, X-linked 4's UMLS CUI is recorded as C0795888[9].
- autism, susceptibility to, X-linked 4's UMLS CUI is recorded as C2931311[10].
- autism, susceptibility to, X-linked 4's GARD rare disease ID is recorded as 3775[11].
- autism, susceptibility to, X-linked 4's Mondo ID is recorded as MONDO_0010440[12].
- autism, susceptibility to, X-linked 4's UniProt disease ID is recorded as DI-04536[13].