Phenotypes for disease #01129 (MRX41 (mental retardation, X-linked, type 41 (MRX41)), OMIM:300849)

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AscendingPhenotype ID     

Phenotype details     

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Age/Diagnosis     

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Individual ID     
0000272286 Macrocephaly, Abnormal location of ears, Low-set ears, Delayed speech and language development, Hyperpigmentation of the skin, Abnormality of skin pigmentation, Hypopigmentation of the skin, Global developmental delay, Abnormal foot morphology, Pes planus, Neurological speech impairment, Language impairment, Abnormality of skin morphology, Neurodevelopmental delay, Increased head circumference - - Familial, X-linked 04y - - - - - Andreas Laner 00377102
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