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] |
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HP:0000010 | Recurrent urinary tract infections | "Repeated infections of the urinary tract." [HPO:curators] |
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HP:0000155 | Oral ulcers | |
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HP:0000206 | Glossitis | "Inflammation of the tongue." [HPO:sdoelken] |
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HP:0000708 | Behavioural/Psychiatric Abnormality | |
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HP:0000737 | Irritability | |
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HP:0000980 | Pallor | |
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HP:0001249 | Mental retardation | |
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HP:0001250 | Seizures | "Seizures are an intermittent `abnormality of the central nervous system` (FMA:HP:0002011) due to a sudden, excessive, disorderly discharge of cerebral neurons and characterized clinically by some combination of disturbance of sensation, loss of consciousness, impairment of psychic function, or convulsive movements." [HPO:probinson] |
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HP:0001251 | Ataxia | "Ataxia is a nonspecific neurological sign and symptom consisting of gross lack of coordination of muscle movements. Ataxia is caused by dysfunction of one or more parts of the nervous system including the cerebellum, the sensory nervous system, the vestibular system, or the cerebral cortex." [HPO:curators] |
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HP:0001252 | Muscular hypotonia | "Muscular hypotonia is an abnormally low muscle tone (the amount of tension or resistance to movement in a muscle), often involving reduced muscle strength. Hypotonia is characterized by a diminished resistance to passive stretching." [HPO:curators] |
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HP:0001263 | Developmental retardation | "A delay in the achievement of motor or mental milestones manifested prior to age 18 and generally associated with lifelong mental and/or physical impairments." [HPO:curators] |
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HP:0001290 | Generalized hypotonia | "Generalized muscular hypotonia (abnormally low muscle tone)." [HPO:curators] |
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HP:0001347 | Hyperreflexia | "The presence of overactive or overresponsive reflexes." [HPO:curators] |
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HP:0001508 | Failure to thrive | |
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HP:0001873 | Thrombocytopenia | |
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HP:0001875 | Neutropenia | |
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HP:0001876 | Pancytopenia | |
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HP:0001880 | Eosinophilia | "Increased count of eosinophile granulocytes in the blood." [HPO:sdoelken] |
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HP:0001882 | Leukopenia | |
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HP:0001889 | Megaloblastic anemia | |
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HP:0002014 | Diarrhea | |
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HP:0002017 | Nausea and vomiting | |
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HP:0002020 | Gastroesophageal reflux | |
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HP:0002024 | Malabsorption | |
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HP:0002039 | Anorexia | |
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HP:0002135 | Basal ganglia calcification | "Calcification affecting one or more structures of the basal ganglia." [HPO:curators] |
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HP:0002205 | Recurrent respiratory infections | |
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HP:0002305 | Athetosis | "Athetosis (from the Greek word for changeable or unfixed ) refers to an inability to sustain the muscles of the fingers, toes, tongue, or any other group of muscles in a fixed position. Instead, posture is interrupted by slow, purposeless involuntary movements." [HPO:curators] |
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HP:0002514 | Cerebral calcification | "The presence of calcification within brain structures." [HPO:curators] |
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HP:0002719 | Recurrent infections | |
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HP:0002721 | Immunodeficiency | |
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HP:0003202 | Amyotrophy | "The presence of muscular atrophy (which is also known as amyotrophy)." [HPO:curators] |
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HP:0003593 | Early onset | |
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HP:0004313 | Reduced immunoglobulin levels | |
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HP:0004851 | folate-responsive megaloblastic anemia | |
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HP:0008872 | Feeding problems in infancy | |
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HP:0009830 | Peripheral neuropathy | "Peripheral neuropathy is a general term for any disorder of the peripheral nervous system. The main clinical features used to classify peripheral neuropathy are distribution, type (mainly demyelinating versus mainly axonal), duration, and course." [HPO:curators] |
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HP:0100660 | Dyskinesis | "A movement disorder which consists of effects including diminished voluntary movements and the presence of involuntary movements." [HPO:sdoelken] |
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HP:0100825 | Cheilitis | "Inflammation of the lip." [HPO:sdoelken] |
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