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1 OMIM reference -
1 associated gene
7 signs/symptoms
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
10 signs/symptoms
Adenine phosphoribosyltransferase deficiency
Hereditary cerebral hemorrhage with amyloidosis, Iowa type

APRT APP


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
APRT
(0.56)
APP



Citations in the biomedical literature:


Adenine phosphoribosyltransferase deficiency
APRT
Hereditary cerebral hemorrhage with amyloidosis, Iowa type
APP



Adenine phosphoribosyltransferase deficiency
Hereditary cerebral hemorrhage with amyloidosis, Iowa type

Synonym(s):
- 2,8-dihydroxyadenine urolithiasis
- APRT deficiency

Synonym(s):
- HCHWA, Iowa type

Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare renal disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
(no data available)

Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: variable
Average age of death: normal
Type of inheritance: autosomal recessive
Epidemiological data:
(no data available)

External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references

Adenine phosphoribosyltransferase deficiency
Hereditary cerebral hemorrhage with amyloidosis, Iowa type

Very frequent
- Autosomal recessive inheritance
- Urinary / renal lithiasis / kidney stones / nephritic colic

Frequent
- Hematuria / microhematuria
- Renal disease / nephropathy

Occasional
- Pollakiuria / polyuria / dysuria / anuria / acute urine retention / oliguria
- Recurrent urinary infections
- Renal failure


Very frequent
- Abnormal gait
- Autosomal dominant inheritance
- Cerebral vascular anomalies
- Feeding disorder / dysphagia / swallowing / sucking disorder / esophageal dyskinesia
- Intracranial / cerebral / meningeal hemorrhage
- Myoclonus / fasciculations
- Psychic / behavioural troubles
- Psychic / psychomotor regression / dementia / intellectual decline
- Transient cerebral ischemia / stroke
- Troubles of memory / amnesia / hypermnesia