Phenotypes for disease #01938 (MPS4B (mucopolysaccharidosis, type IVB (MPS4B)), OMIM:253010)

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     

Protein     

Owner     

Individual ID     
0000232563 HP:0003330 Abnormal bone structure HP:0001999 Abnormal facial shape HP:0000943 Dysostosis multiplex HP:000320 Skeletal muscle atrophy - - Familial, autosomal recessive - 13y 13y - - Sarah Snanoudj 00306729
0000232914 HP:0001999 Abnormal facial shape HP:0000943 Dysostosis multiplex - - Familial, autosomal recessive - 07y 07y - - Sarah Snanoudj 00307108
0000297668 Motor delay, Elevated serum acid phosphatase, Elevated circulating alkaline phosphatase concentration, Ganglioside accumulation, Elevated alkaline phosphatase of bone origin, Beta-galactosidase deficiency - - Familial, autosomal recessive 00y04m - - - - Andreas Laner 00405119
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