Fibroblast metachromasia

Symptom Information:

Symptom ID: HPO:0003610
Synonyms:
Fibroblast metachromasia [OMIM:Fibroblast metachromasia]
Quality:
Cross references:
OMIM: "Fibroblast metachromasia" [OMIM:Fibroblast metachromasia]
Is a (Direct Parents):
HPO         Cellular metachromasia
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          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)
                      Cellular metachromasia(HPO:0003653)
                         Fibroblast metachromasia(HPO:0003610)
MedDRA:
Database Frequency: 3 / 7739
Resource:

All diseases associated with this symptom:

MORQUIO SYNDROME C (OMIM:252300)
MUCOPOLYSACCHARIDOSES, UNCLASSIFIED TYPES (OMIM:252700)
Mucopolysaccharidosis type 4 (Orphanet:582)