Hyperlysinuria

Symptom Information:

Symptom ID: HPO:0003297
Synonyms:
Lysinuria [HPO:0003297]
Hyperlysinuria [OMIM:Hyperlysinuria]
Lysinuria [OMIM:Lysinuria]
Quality:
Cross references:
OMIM: "Hyperlysinuria" [OMIM:Hyperlysinuria]
OMIM: "Lysinuria" [OMIM:Lysinuria]
Is a (Direct Parents):
HPO         Aminoaciduria
HPO         Abnormality of lysine metabolism
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the genitourinary system(HPO:0000119)
          Abnormality of the urinary system(HPO:0000079)
             Abnormality of the urinary system physiology(HPO:0011277)
                Abnormality of urine homeostasis(HPO:0003110)
                   Aciduria(HPO:0012072)
                      Aminoaciduria(HPO:0003355)
                         Hyperlysinuria(HPO:0003297)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Abnormality of urine homeostasis(HPO:0003110)
             Aciduria(HPO:0012072)
                Aminoaciduria(HPO:0003355)
                   Hyperlysinuria(HPO:0003297)
          Abnormality of carboxylic acid metabolism(HPO:0004354)
             Abnormality of amino acid metabolism(HPO:0004337)
                Abnormality of aspartate family amino acid metabolism(HPO:0010899)
                   Abnormality of lysine metabolism(HPO:0010908)
                      Hyperlysinuria(HPO:0003297)
                Aminoaciduria(HPO:0003355)
                   Hyperlysinuria(HPO:0003297)
MedDRA:
Database Frequency: 10 / 7739
Resource:

All diseases associated with this symptom:

Cystinuria (Orphanet:214)
Cystinuria type A (Orphanet:93612)
Cystinuria type B (Orphanet:93613)
DIAMINOPENTANURIA (OMIM:222350)
HYPERLYSINURIA WITH HYPERAMMONEMIA (OMIM:238750)
Hyperdibasic aminoaciduria type 1 (Orphanet:1032)
Hyperlysinemia, type I (OMIM:238700)
LYSINE MALABSORPTION SYNDROME (OMIM:247950)
Saccharopinuria (Orphanet:3124)
Seizures - intellectual deficit due to hydroxylysinuria (Orphanet:79156)