Phenotypes for disease #00819 (AUTSX2 (mental retardation, X-linked (MRXS)), OMIM:300495)

3 entries on 1 page. Showing entries 1 - 3.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Birth_Details     

Protein     

Owner     

Individual ID     
0000157240 global developmental delay (HP:0001263), autistic behavior (HP:0000729) - - Isolated (sporadic) 03y07m 03y07m - - - - Ke Xu 00208613
0000254875 (+) Macrocephaly,(+) Low-set ears,(+) Nevus flammeus,(+) Motor delay,(+) Short foot,(+) Nevus flammeus of the forehead,(+) Neurodevelopmental delay,(+) Small hand - - Unknown 00y09m - - - - - Andreas Laner 00359603
0000270732 (+) Microcephaly,(+) Seizure,(+) Polymicrogyria,(+) Abnormal cortical gyration,(+) Aplasia/Hypoplasia of the cerebrum,(+) Abnormal nervous system physiology,(+) Decreased head circumference - - Familial, X-linked dominant 00y06m - - - - - Andreas Laner 00375518
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