Dermatan sulfate excretion in urine

Symptom Information:

Symptom ID: HPO:0008301
Synonyms:
Dermatan sulfate excretion in urine [OMIM:Dermatan sulfate excretion in urine]
Quality:
Cross references:
OMIM: "Dermatan sulfate excretion in urine" [OMIM:Dermatan sulfate excretion in urine]
Is a (Direct Parents):
HPO         Mucopolysacchariduria
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Abnormality of urine homeostasis(HPO:0003110)
             Urinary glycosaminoglycan excretion(HPO:0003541)
                Mucopolysacchariduria(HPO:0008155)
                   Dermatan sulfate excretion in urine(HPO:0008301)
          Abnormality of carbohydrate metabolism/homeostasis(HPO:0011013)
             Abnormality of polysaccharide metabolism(HPO:0011012)
                Abnormality of glycosaminoglycan metabolism(HPO:0004371)
                   Abnormality of mucopolysaccharide metabolism(HPO:0011020)
                      Mucopolysacchariduria(HPO:0008155)
                         Dermatan sulfate excretion in urine(HPO:0008301)
                   Urinary glycosaminoglycan excretion(HPO:0003541)
                      Mucopolysacchariduria(HPO:0008155)
                         Dermatan sulfate excretion in urine(HPO:0008301)
       Abnormality of the genitourinary system(HPO:0000119)
          Abnormality of the urinary system(HPO:0000079)
             Abnormality of the urinary system physiology(HPO:0011277)
                Abnormality of urine homeostasis(HPO:0003110)
                   Urinary glycosaminoglycan excretion(HPO:0003541)
                      Mucopolysacchariduria(HPO:0008155)
                         Dermatan sulfate excretion in urine(HPO:0008301)
MedDRA:
Database Frequency: 8 / 7739
Resource:

All diseases associated with this symptom:

Hurler syndrome (Orphanet:93473)
Hurler-Scheie syndrome (Orphanet:93476)
Mucopolysaccharidosis type 2 (Orphanet:580)
Mucopolysaccharidosis type 2, attenuated form (Orphanet:217093)
Mucopolysaccharidosis type 2, severe form (Orphanet:217085)
Mucopolysaccharidosis type 6 (Orphanet:583)
Mucopolysaccharidosis type 7 (Orphanet:584)
Scheie syndrome (Orphanet:93474)