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DOID:0060808 - syndromic X-linked intellectual disability 7
Disease Ontology Definition:A syndromic X-linked intellectual disability characterized by intellectual deficit, obesity, hypogonadism, and tapering fingers that has_material_basis_in variation in the chromosome region Xp11.3-q22.
Synonyms: MRXS7, X-linked intellectual disability, Ahmad type, mental retardation, X-linked syndromic 7,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0010270 - syndromic X-linked intellectual disability 7 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee