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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
achondrogenesis type IB 
acquired mineral metabolism disease 
atelosteogenesis type II 
calcium metabolic disease +   
chondrodysplasia with joint dislocations, gPAPP type 
COASY protein-associated neurodegeneration 
diastrophic dysplasia 
Fatal multiple mitochondrial dysfunction syndrome +  
iron metabolism disease +   
multiple epiphyseal dysplasia type 4 
phosphorus metabolism disease +   
potassium deficiency disease +   
spondyloepimetaphyseal dysplasia, PAPSS2 type 
spondyloepiphyseal dysplasia with congenital joint dislocations 
sulfur metabolism disease +  
A disease that has its basis in the disruption of sulfur compound metabolic process.

Synonyms
Exact Synonyms: disorder of sulfur compound metabolic process ;   disorder of sulfur metabolic process ;   disorder of sulfur metabolism ;   disorder of sulphur compound metabolic process ;   disorder of sulphur metabolic process ;   disorder of sulphur metabolism ;   sulfur compound metabolic process disease ;   sulphur compound metabolic process disease
Alternate IDs: MONDO:0056803
Xrefs: MEDGEN:688004 ;   SCTID:123809005 ;   UMLS:C1263724
Definition Sources: MONDO:patterns/disrupts_process

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