HP:0000006 | Autosomal dominant 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 heterozygotes. In the context of medical genetics, an autosomal dominant disorder is caused when a single copy of the mutant allele is present. Males and females are affected equally, and can both transmit the disorder with a risk of 50% for each child of inheriting the mutant allele." [HPO:curators] |
Show
|
HP:0000293 | Full cheeks | |
Show
|
HP:0000483 | Astigmatism | |
Show
|
HP:0000490 | Deep set eyes | |
Show
|
HP:0000540 | Hypermetropia | |
Show
|
HP:0000565 | Esotropia | |
Show
|
HP:0000639 | Nystagmus | "Rhythmic, involuntary oscillations of one or both eyes related to abnormality in fixation, conjugate gaze, or vestibular mechanisms." [HPO:curators] |
Show
|
HP:0000750 | Impaired language development | |
Show
|
HP:0001249 | Mental retardation | |
Show
|
HP:0001258 | Spastic paraplegia | |
Show
|
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] |
Show
|
HP:0001338 | Partial agenesis of the corpus callosum | "A partial failure of the development of the corpus callosum." [HPO:curators] |
Show
|
HP:0001347 | Hyperreflexia | "The presence of overactive or overresponsive reflexes." [HPO:curators] |
Show
|
HP:0002059 | Cerebral atrophy | |
Show
|
HP:0002509 | Limb hypertonia | |
Show
|
HP:0003593 | Early onset | |
Show
|
HP:0006956 | Dilation of lateral ventricles | |
Show
|
HP:0007663 | Decreased central vision | |
Show
|
HP:0008936 | Muscular hypotonia of the trunk | "Muscular hypotonia (abnormally low muscle tone) affecting the musculature of the trunk." [HPO:curators] |
Show
|
HP:0011220 | Prominent forehead | "Forward prominence of the entire forehead, due to protrusion of the frontal bone." [pmid:19125436] |
Show
|
HP:0012448 | Delayed myelination | "`Delayed` (PATO:0000502) `myelination` (GO:0042552)." [ORCID:0000-0001-5208-3432] |
Show
|