Phenotypes for disease #05325 (MRXS35 (mental retardation, X-linked, syndromic, type 35 (MRXS-35)), OMIM:300998)

2 entries on 1 page. Showing entries 1 - 2.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000350693 see paper; ..., fetal growth delay, development delay, feeding difficulties, congenital laryngeal stridor, neonatal pneumonia, neonatal hypoglycemia, craniofacial anomalies, cryptorchidism - MRXS35 Isolated (sporadic) 00y02m - fetal growth delay - Ke Wu 00464560
0000366931 see paper; ..., feeding difficulties, congenital laryngeal stridor, neonatal pneumonia, neonatal hypoglycemia, intellectual disability, psychomotor development delay, speech delay, short stature, craniofacial anomalies, cryptorchidism - MRXS35 Isolated (sporadic) 09y - fetal growth delay - Ke Wu 00484153
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