Clinical Signs and Symptoms
ORPHA:3226 Deafness-lymphedema-leukemia syndrome
The phenotypic description of this disease is based on an analysis of the biomedical literature and uses the terms of the Human Phenotype Ontology (HPO). Phenotypic abnormalities are presented by order of frequency of occurrence in the patient population, then by alphabetical order inside each frequency group.
- Abnormal neutrophil count HP:0011991
- Acute leukemia HP:0002488
- Bone marrow hypocellularity HP:0005528
- Fatigue HP:0012378
- Lymphedema HP:0001004
- Neurological speech impairment HP:0002167
- Prolonged bleeding time HP:0003010
- Respiratory failure HP:0002878
- Sensorineural hearing impairment HP:0000407
- Thrombocytopenia HP:0001873
- Abnormality of the optic nerve HP:0000587
- Bruising susceptibility HP:0000978
- Chronic otitis media HP:0000389
- Fever HP:0001945
- Hepatomegaly HP:0002240
- Hypercoagulability HP:0100724
- Intracranial hemorrhage HP:0002170
- Migraine HP:0002076
- Nausea and vomiting HP:0002017
- Pallor HP:0000980
- Recurrent respiratory infections HP:0002205
- Splenomegaly HP:0001744
- Vertigo HP:0002321
- Visual loss HP:0000572
- Weight loss HP:0001824
Specialised Social Services
The information provided is based on published scientific articles.
The information provided is estimated for the entire population of patients in routine care. Some phenotypic abnormalities reported here may occur individually with a variable temporality or severity, while others, not listed, may still be encountered. Phenotypic annotations are not yet available for all rare diseases; the annotation process is ongoing.
The information contained in Orphanet is regularly updated. It is possible that discoveries have been made since the last update and have not yet been incorporated.
Professionals are encouraged to always consult the latest scientific publications before making a decision based on the information provided. The information contained in Orphanet is not intended to replace the services of a healthcare professional. Orphanet cannot be held responsible for the deleterious, truncated or erroneous use of any information found in the Orphanet database.