HP:0000007 | Autosomal recessive inheritance | "A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in homozygotes. In the context of medical genetics, autosomal recessive disorders manifest in homozygotes (with two copies of the mutant allele) or compound heterozygotes (whereby each copy of a gene has a distinct mutant allele)." [HPO:curators] |
Show
|
HP:0000083 | Renal failure | |
Show
|
HP:0000093 | Proteinuria | |
Show
|
HP:0000097 | Focal segmental glomerulosclerosis | |
Show
|
HP:0000100 | Nephrotic syndrome | |
Show
|
HP:0000112 | Nephropathy | "A nonspecific term referring to disease or damage of the kidneys." [HPO:curators] |
Show
|
HP:0000225 | Gingival bleeding | |
Show
|
HP:0000726 | Dementia | |
Show
|
HP:0000790 | Hematuria | "The presence of blood in the urine. Hematuria may be gross hematuria (visible to the naked eye) or microscopic hematuria (detected by dipstick or microscopic examination of the urine)." [HPO:curators] |
Show
|
HP:0000823 | Delayed puberty | |
Show
|
HP:0000938 | Osteopenia | "Osteopenia refers to a reduction in bone mineral density (BMD) below normal peak BMD but not low enough to be classified as osteoporosis. According to the WHO, osteopenia is characterized by a value of BMD more than 1 standard deviation below the young adult mean, but less than 2 standard deviations below this value." [HPO:curators] |
Show
|
HP:0000978 | Ecchymoses | |
Show
|
HP:0000992 | Photosensitivity | "An increased sensitivity of the skin to light. Photosensitivity may result in a rash upon exposure to the sun (which is known as photodermatosis). Photosensitivity can be diagnosed by phototests in which light is shone on small areas of skin." [HPO:curators] |
Show
|
HP:0001249 | Mental retardation | |
Show
|
HP:0001260 | Dysarthria | "Dysarthric speech is a general description referring to a neurological speech disorder characterized by poor articulation. Depending on the involved neurological structures, dysarthria may be further classified as spastic, flaccid, ataxic, hyperkinetic and hypokinetic, or mixed." [HPO:curators] |
Show
|
HP:0001272 | Cerebellar atrophy | |
Show
|
HP:0001336 | Myoclonus | "Very brief, involuntary random muscular contractions occurring at rest, in response to sensory stimuli, or accompanying voluntary movements." [HPO:curators] |
Show
|
HP:0001394 | Cirrhosis | |
Show
|
HP:0001541 | Ascites | |
Show
|
HP:0001637 | Abnormality of the myocardium | |
Show
|
HP:0001698 | Pericardial effusion | |
Show
|
HP:0001744 | Splenomegaly | "An abnormal enlargement of the spleen." [HPO:curators] |
Show
|
HP:0001873 | Thrombocytopenia | |
Show
|
HP:0001876 | Pancytopenia | |
Show
|
HP:0001882 | Leukopenia | |
Show
|
HP:0001903 | Anemia | |
Show
|
HP:0001971 | Hypersplenism | |
Show
|
HP:0002015 | Dysphagia | "Difficulty in swallowing." [HPO:curators] |
Show
|
HP:0002027 | Abdominal pain | |
Show
|
HP:0002039 | Anorexia | |
Show
|
HP:0002066 | Gait ataxia | "Impairment of the ability to coordinate the movements required for normal walking." [HPO:curators] |
Show
|
HP:0002070 | Limb ataxia | |
Show
|
HP:0002080 | Intention tremor | "An oscillatory cerebellar ataxia that tends to be absent when the limbs are inactive and during the first part of voluntary movement but worsening as the movement continues and greater precision is required (e.g., in touching a target such as the patient s nose or a physician s finger)." [HPO:curators] |
Show
|
HP:0002092 | Pulmonary hypertension | |
Show
|
HP:0002174 | Postural tremor | "A type of tremors that is triggered by holding a limb in a fixed position." [HPO:curators] |
Show
|
HP:0002197 | Generalized seizures | "Recurrent generalized `seizures` (HP:0001250), that is seizures that affect both cerebral hemispheres from the start of the seizure, producing loss of consciousness." [HPO:probinson] |
Show
|
HP:0002240 | Hepatomegaly | "An abnormal enlargment of the liver." [HPO:curators] |
Show
|
HP:0002392 | EEG shows 3-4-Hz spike and multispike slow wave complexes | |
Show
|
HP:0002653 | Bone pain | |
Show
|
HP:0002750 | Delayed skeletal maturation | "A decreased rate of skeletal maturation. Delayed skeletal maturation can be diagnosed on the basis of an estimation of the bone age from radiographs of specific bones in the human body." [HPO:curators] |
Show
|
HP:0002756 | Pathologic fracture | "A pathologic fracture occurs when a bone breaks in an area that is weakened secondary to another disease process such as tumor, infection, and certain inherited bone disorders. A pathologic fracture can occur without a degree of trauma required to cause fracture in healthy bone." [HPO:curators] |
Show
|
HP:0002758 | Osteoarthritis | |
Show
|
HP:0002797 | Osteolysis | |
Show
|
HP:0002808 | Kyphosis | |
Show
|
HP:0002953 | Vertebral compression fractures | |
Show
|
HP:0003678 | Rapidly progressive | |
Show
|
HP:0005230 | Biliary tract obstruction | |
Show
|
HP:0006530 | Interstitial pulmonary disease | |
Show
|
HP:0007000 | Morning myoclonic jerks | |
Show
|
HP:0010702 | Increased immunoglobulin level | "An abnormally increased level of immunoglobulin in blood." [HPO:probinson] |
Show
|
HP:0010741 | Edema of the lower limbs | |
Show
|
HP:0010885 | Aseptic necrosis | "A disease where there is cellular death (necrosis) of bone components due to interruption of the blood supply." [HPO:sdoelken] |
Show
|
HP:0011001 | Increased bone mineral density | "An abnormal increase of bone mineral density, that is, of the amount of matter per cubic centimeter of bones which is often refered to as osteosclerosis. Osteosclerosis can be detected on radiological examination as an increased whiteness (density) of affected bones." [HPO:curators] |
Show
|