| 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: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:0000174 | Abnormality of palate | "Any abnormality of the `palate` (FMA:54549), i.e., of roof of the mouth)." [HPO:probinson] |
Show
|
| HP:0000218 | High palate | "Height of the palate more than 2 SD above the mean (objective) or palatal height at the level of the first permanent molar more than twice the height of the teeth (subjective)." [pmid:19125428] |
Show
|
| HP:0000311 | Round face | "An unusually round appearance of the face." [HPO:curators] |
Show
|
| HP:0000347 | Mandibular hypoplasia | "Underdevelopment of the mandible." [HPO:curators] |
Show
|
| HP:0000411 | Protruding ears | |
Show
|
| HP:0000470 | Short neck | |
Show
|
| HP:0000473 | Torticollis | |
Show
|
| HP:0000565 | Esotropia | |
Show
|
| HP:0000975 | Hyperhidrosis | "An abnormally increased perspiration." [HPO:probinson] |
Show
|
| HP:0001181 | Adducted thumbs | |
Show
|
| HP:0001238 | Slender fingers | "Digits are disproportionaly narrow (reduced girth)." [HPO:curators] |
Show
|
| HP:0001270 | Motor retardation | |
Show
|
| HP:0001290 | Generalized hypotonia | "Generalized muscular hypotonia (abnormally low muscle tone)." [HPO:curators] |
Show
|
| HP:0001319 | Neonatal hypotonia | "Muscular hypotonia (abnormally low muscle tone) manifesting in the neonatal period." [HPO:curators] |
Show
|
| HP:0001371 | Contractures | |
Show
|
| HP:0001387 | Joint stiffness | "Joint stiffness is a perceived sensation of tightness in a joint or joints when attempting to move them after a period of inactivity. Joint stiffness typically subsides over time." [HPO:curators] |
Show
|
| HP:0001388 | Joint laxity | |
Show
|
| HP:0001508 | Failure to thrive | |
Show
|
| HP:0001533 | Asthenic habitus | "Asthenic habitus refers to a slender build with long limbs, an angular profile, and prominent muscles or bones." [HPO:curators] |
Show
|
| HP:0001558 | Decreased fetal movement | "An abnormal reduction in quantity or strength of fetal movements." [HPO:curators] |
Show
|
| HP:0001626 | Abnormality of the cardiovascular system | "Any abnormality of the heart or vasculature." [HPO:curators] |
Show
|
| HP:0001762 | Talipes equinovarus | "Also called clubfoot typically has 4 main components: inversion and adduction of the forefoot; inversion of the heel and hindfoot; equinus (limitation of extension) of the ankle and subtalar joint; and internal rotation of the leg. Clubfoot is a complex, multifactorial deformity with genetic and intrauterine factors. One popular theory postulates that a clubfoot is a result of intrauterine maldevelopment of the talus that leads to adduction and plantarflexion of the foot. On radiographic projection a clubfoot can be noted as parallel axes of talus and calcaneus." [HPO:curators] |
Show
|
| HP:0001771 | Achilles tendon contractures | |
Show
|
| HP:0002359 | Frequent falls | |
Show
|
| HP:0002460 | Distal muscle weakness | "Reduced strength of the distal musculature." [HPO:curators] |
Show
|
| HP:0002650 | Scoliosis | "The presence of an abnormal lateral curvature of the spine." [HPO:curators] |
Show
|
| HP:0002747 | Respiratory insufficiency due to muscle weakness | |
Show
|
| HP:0002783 | Recurrent lower respiratory tract infections | |
Show
|
| HP:0002808 | Kyphosis | |
Show
|
| HP:0002827 | Dislocated hips | |
Show
|
| HP:0002877 | Nocturnal hypoventilation | |
Show
|
| HP:0002878 | Early respiratory failure | |
Show
|
| HP:0002938 | Lumbar hyperlordosis | |
Show
|
| HP:0002944 | Thoracolumbar scoliosis | |
Show
|
| HP:0002987 | Elbow contractures | |
Show
|
| HP:0003198 | Myopathy | |
Show
|
| HP:0003202 | Amyotrophy | "The presence of muscular atrophy (which is also known as amyotrophy)." [HPO:curators] |
Show
|
| HP:0003236 | Elevated serum creatine phosphokinase | |
Show
|
| HP:0003306 | Spinal rigidity | |
Show
|
| HP:0003324 | Generalized muscle weakness | "Generalized weakness or decreased strength of the muscles." [HPO:curators] |
Show
|
| HP:0003325 | Limb-girdle muscle weakness | "Weakness of the limb-girdle muscles (also known as the pelvic and shoulder girdles), that is, lack of strength of the muscles around the shoulders and the pelvis." [HPO:curators] |
Show
|
| HP:0003457 | Abnormal EMG findings | "Abnormal results of investigations using electromyography (EMG)." [HPO:curators] |
Show
|
| HP:0003458 | EMG myopathic abnormalities | "The presence of abnormal electromyographic patterns indicative of myopathy, such as small-short polyphasic motor unit potentials." [HPO:curators] |
Show
|
| HP:0003557 | Increased variability in muscle fiber size | "An abnormally high degree of muscle fiber size variation. This phenotypic feature can be observed upon muscle biopsy." [HPO:curators] |
Show
|
| HP:0003593 | Early onset | |
Show
|
| HP:0003621 | Juvenile onset | |
Show
|
| HP:0003676 | Progressive disorder | |
Show
|
| HP:0003677 | Slow progression | |
Show
|
| HP:0003700 | Generalized amyotrophy | "Generalized wasting of loss of muscle tissue." [HPO:curators] |
Show
|
| HP:0003701 | Proximal muscle weakness | "A lack of strength of the proximal muscles." [HPO:curators] |
Show
|
| HP:0003713 | Muscle fiber necrosis | "Abnormal cell death involving muscle fibers usually associated with break in, or absence of, muscle surface fiber membrane and resulting in irreversible damage to muscle fibers." [HPO:curators] |
Show
|
| HP:0003741 | Congenital muscular dystrophy | |
Show
|
| HP:0003803 | Type 1 muscle fiber predominance | "An abnormal predominance of type I muscle fibers (in general, this feature can only be observed on muscle biopsy)." [HPO:curators] |
Show
|
| HP:0003828 | Variable expressivity | |
Show
|
| HP:0004322 | Decreased body height | "A height below that which is expected according to age and gender norms. Although there is no universally accepted definition of short stature, many refer to "short stature" as height more than 2 standard deviations below the mean for age and gender (or below the 3rd percentile for age and gender dependent norms)." [HPO:curators] |
Show
|
| HP:0004326 | Cachexia | |
Show
|
| HP:0005072 | Hyperextensibility at wrists | "The ability of the wrist joints to move beyond their normal range of motion." [HPO:curators] |
Show
|
| HP:0005952 | Decreased pulmonary function | |
Show
|
| HP:0005988 | Torticollis, congenital | |
Show
|
| HP:0005997 | Restricted neck movement due to contractures | |
Show
|
| HP:0006149 | Increased laxity of fingers | |
Show
|
| HP:0006380 | Knee flexion deformities | |
Show
|
| HP:0006460 | Increased laxity of ankles | |
Show
|
| HP:0006466 | Contractures of the ankles | |
Show
|
| HP:0007502 | Follicular hyperkeratosis | |
Show
|
| HP:0008081 | Valgus foot deformity | |
Show
|
| HP:0008180 | Mildly elevated creatine phosphokinase | |
Show
|
| HP:0008872 | Feeding problems in infancy | |
Show
|
| HP:0009025 | Increased connective tissue | "The presence of an abnormally increased amount of connective tissue." [HPO:curators] |
Show
|
| HP:0009113 | Diaphragmatic weakness | |
Show
|
| HP:0010511 | Increased length of toes | "The presence of abnormally long toes." [HPO:curators] |
Show
|
| HP:0010628 | Facial muscle weakness | "A weakness of any or all of the muscles of the face of any etiology." [HPO:curators] |
Show
|
| HP:0100297 | Increased endomysial connective tissue | |
Show
|
| HP:0100490 | Camptodactyly (hands) | "Contractures of one ore more joints of the fingers." [HPO:sdoelken] |
Show
|
