Search on: PROLIDASE DEFICIENCY 
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Descriptor English:   Prolidase Deficiency 
Descriptor Spanish:   Deficiencia de Prolidasa 
Descriptor Portuguese:   Deficiência de Prolidase 
Synonyms English:   Hyperimidodipeptiduria
Imidodipeptidase Deficiency
Deficiencies, Imidodipeptidase
Deficiencies, Prolidase
Deficiency, Imidodipeptidase
Deficiency, Prolidase
Hyperimidodipeptidurias
Imidodipeptidase Deficiencies
Prolidase Deficiencies  
Tree Number:   C16.131.077.735
C16.131.831.720
C16.320.565.100.794
C16.320.850.746
Definition English:   Rare autosomal recessive disorder of metabolism due to mutations in the prolidase gene. It is characterized by recurrent lower extremity skin ulcers, recurrent infections, and FACIES, often with INTELLECTUAL DISABILITY. 
History Note English:   2010 
Allowable Qualifiers English:  
BL blood CF cerebrospinal fluid
CI chemically induced CL classification
CO complications DI diagnosis
DG diagnostic imaging DH diet therapy
DT drug therapy EC economics
EM embryology EN enzymology
EP epidemiology EH ethnology
ET etiology GE genetics
HI history IM immunology
ME metabolism MI microbiology
MO mortality NU nursing
PS parasitology PA pathology
PP physiopathology PC prevention & control
PX psychology RT radiotherapy
RH rehabilitation SU surgery
TH therapy UR urine
VE veterinary VI virology
Record Number:   53554 
Unique Identifier:   D056732 

Occurrence in VHL: 		 

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