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DO Term : spondyloepiphyseal dysplasia Maroteaux type [DOID:0111553] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  An osteochondrodysplasia characterized by dysplastic epiphyses, short stature appearing in infancy, short neck, short and stubby hands and feet, platyspondyly, severe brachydactyly, and pelvic abnormalities that has_material_basis_in heterozygous mutation in the TRPV4 gene on chromosome 12q24.11.
  • synonyms:
  • UMLS_CUI:C3159322,
  • Pseudo-Morquio syndrome type 2,
  • 184095,
  • GARD:994,
  • Brachyolmia Type 2,
  • ORDO:263482,
  • SNOMEDCT_US_2023_03_01:719204007,
  • OMIM:184095,
  • SED, Maroteaux type,
  • spondyloepiphyseal dysplasia of Maroteaux
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Ontology

Ontology Term --> All ancestors

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Ontology Term --> Direct children

Ontology Term --> Direct parents