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Hemolytic anemia due to adenylate kinase deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Hereditary cerebral hemorrhage with amyloidosis, Iowa type
1 OMIM reference -
1 associated gene
10 signs/symptoms
Hemolytic anemia due to adenylate kinase deficiency
Hereditary cerebral hemorrhage with amyloidosis, Iowa type

AK1
(UniProt - OMIM)
 APP
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
AK1
(0.56)
APP


Citations in the biomedical literature:


Hemolytic anemia due to adenylate kinase deficiency
AK1
Hereditary cerebral hemorrhage with amyloidosis, Iowa type
APP



Hemolytic anemia due to adenylate kinase deficiency
Hereditary cerebral hemorrhage with amyloidosis, Iowa type

Synonym(s):
(no synonyms)

Synonym(s):
- HCHWA, Iowa type
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
Hereditary cerebral hemorrhage with amyloidosis, Iowa type

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



Hemolytic anemia due to adenylate kinase deficiency

(no data available)