Phenotypes for disease #05302 (MPS1 (mucopolysaccharidosis, type I (MPS-1)))

7 entries on 1 page. Showing entries 1 - 7.
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AscendingPhenotype ID     

Phenotype details     

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Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000084637 Mucopolysaccharidosis type I; MPS I - - Familial, autosomal recessive - - - - Gerard C.P. Schaafsma 00106839
0000084639 Mucopolysaccharidosis type I; MPS I - - Familial, autosomal recessive - - - - Gerard C.P. Schaafsma 00106841
0000084665 Mucopolysaccharidosis type I; MPS I - - Familial, autosomal recessive - - - - Gerard C.P. Schaafsma 00106867
0000084667 clinical and biochemical confirmed MPS type I - - Isolated (sporadic) - - - - Alexander Volk 00106869
0000143836 11m diagnosed; 12y cognitive level of 8y after stem cell transplant mucopolysaccharidosis, type I MPS-1H Familial, autosomal recessive - - - - Marianne Hoogeveen-Westerveld 00183080
0000257666 - Usher syndrome Scheie syndrome Familial, autosomal recessive - - - - Barbara Vona 00362252
0000337680 macrocephaly with coarse features, short stature, short neck, tongue enlargement, hepatomegaly, joint contracture, claw hand deformity, umbilical hernia, dorsal kyphosis, a large Mongolian spot on the back, cloudy cornea, macroglossia, and irregular teeth - - Isolated (sporadic) 08y - - - Lulu Yan 00448493
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