Concept information
Término preferido
Hyalinosis, Systemic
Notice: Undefined index: in /var/www/html/model/Concept.php on line 545
Tipo
-
mesh:Descriptor
Definición
- Autosomal recessive disorder characterized by HYALINE deposition in the skin, bone, gastrointestinal tract, muscles and glands; multiple subcutaneous skin nodules; GINGIVAL HYPERTROPHY; and joint CONTRACTURES. Mutations in the capillary morphogenesis protein-2 are associated with the disorder.
Concepto genérico
Etiquetas alternativas
- Fibromatosis Hyalinica Multiplex Juvenilis
- Fibromatosis Juvenile Hyaline
- Fibromatosis, Juvenile Hyaline
- Hyaline Fibromatosis Juvenile
- Hyaline Fibromatosis Syndrome
- Hyalinosis, Systemic Juvenile
- Infantile Systemic Hyalinosis
- Juvenile Hyaline Fibromatosis
- Juvenile Hyalinosis
- Murray Syndrome
- Puretic Syndrome
- Systemic Hyalinosis
En otras lenguas
-
francés
-
Syndrome de la fibromatose hyaline
URI
http://data.loterre.fr/ark:/67375/JVR-XJ61GNCZ-C
{{label}}
{{#each values }} {{! loop through ConceptPropertyValue objects }}
{{#if prefLabel }}
{{/if}}
{{/each}}
{{#if notation }}{{ notation }} {{/if}}{{ prefLabel }}
{{#ifDifferentLabelLang lang }} ({{ lang }}){{/ifDifferentLabelLang}}
{{#if vocabName }}
{{ vocabName }}
{{/if}}