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] |
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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:0000023 | Inguinal hernia | |
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HP:0000028 | Cryptorchidism | "Absence of one or both testes from the scrotum owing to failure of the testis or testes to descend through the inguinal canal to the testis." [HPO:curators] |
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HP:0000160 | Microstomia | "The presence of an abnormally small `mouth` (FMA:49184)." [HPO:curators] |
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HP:0000164 | Abnormality of the teeth | "Any abnormality of the primary (deciduous) or permanent teeth." [HPO:curators] |
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HP:0000175 | Cleft palate | "Cleft palate is a developmental defect of the `palate` (FMA:54549) resulting from a failure of fusion of the palatine processes." [HPO:curators] |
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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] |
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HP:0000252 | Microcephaly | "Microcephaly is a neurodevelopmental disorder in which the circumference of the head is more than two standard deviations smaller than the age- and gender-dependent norm." [HPO:curators] |
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HP:0000272 | Malar hypoplasia | "Underdeveloped midface region." [HPO:curators] |
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HP:0000275 | Narrow face | |
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HP:0000286 | Epicanthus | "An epicanthal fold is a semilunar fold of skin that extends from the upper eyelid across the medial canthal area to the lower eyelid." [HPO:curators] |
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HP:0000298 | Mask-like facies | |
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HP:0000303 | Mandibular prognathia | "Abnormal prominence of the chin related to an abnormally long mandible." [HPO:curators] |
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HP:0000316 | Hypertelorism | |
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HP:0000325 | Triangular facies | |
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HP:0000343 | Long philtrum | |
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HP:0000346 | Whistling Appearance | |
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HP:0000347 | Mandibular hypoplasia | "Underdevelopment of the mandible." [HPO:curators] |
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HP:0000365 | Hearing loss | |
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HP:0000368 | Low-set, posteriorly rotated ears | |
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HP:0000411 | Protruding ears | |
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HP:0000430 | Hypoplastic nasal alae | "Thinned, deficient, or excessively arched `ala nasi` (FMA:59519)." [pmid:19152422] |
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HP:0000431 | Broad nasal bridge | "Increased horizontal dimension of the upper, bony part of the nose." [HPO:curators] |
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HP:0000457 | Flat nose | |
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HP:0000465 | Webbed neck | |
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HP:0000470 | Short neck | |
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HP:0000486 | Strabismus | "Strabismus (also known as squint) is a condition in which the eyes are not properly aligned with each other." [HPO:curators] |
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HP:0000490 | Deep set eyes | |
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HP:0000494 | Downward slanting palpebral fissures | |
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HP:0000506 | Telecanthus | "An abnormally increased distance between the medial canthi (angle between eyelids) of the eyelids." [HPO:curators] |
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HP:0000508 | Ptosis | "Drooping of the eyelid." [HPO:curators] |
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HP:0000581 | Blepharophimosis | "Reduced width of the palpebral fissures." [HPO:sdoelken] |
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HP:0000598 | Abnormality of the ears | |
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HP:0000951 | Abnormality of the skin | "An abnormality of the `skin` (FMA:7163)." [HPO:probinson] |
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HP:0001040 | Multiple pterygia | |
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HP:0001181 | Adducted thumbs | |
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HP:0001193 | Ulnar deviation of the hand or of fingers of the hand | |
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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:0001272 | Cerebellar atrophy | |
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HP:0001324 | Muscle weakness | "Reduced strength of muscles." [HPO:curators] |
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HP:0001363 | Craniosynostosis | "Craniosynostosis refers to the premature closure of the cranial sutures. Primary craniosynostosis refers to the closure of one or more sutures due to abnormalities in skull development, and secondary craniosynostosis results from failure of brain growth." [HPO:curators] |
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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] |
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HP:0001508 | Failure to thrive | |
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HP:0001518 | Low birth weight | |
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HP:0001557 | Prenatal movement abnormality | |
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HP:0001561 | Polyhydramnios | |
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HP:0001562 | Oligohydramnios | |
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HP:0001611 | Nasal speech | |
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HP:0001623 | breech presentation | |
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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] |
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HP:0001838 | Vertical talus | |
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HP:0001840 | Metatarsus varus | "Metatarsus varus (adductus) is one of the most common foot deformities, that is defined as a transverse plane deformity in Lisfranc s (tarsometatarsal) joints in which the metatarsals are deviated medially. The relationship between talus and calcaneus is normal. On inspection the toes angle abruptly towards the midline, creating a C-shaped lateral foot border with a prominent styloid process of the 5th metatarsal. The result is that the forefoot is twisted inwards relative to the heel, so that the sole faces the midline." [HPO:curators] |
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HP:0001848 | Calcaneovalgus deformities | |
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HP:0001883 | Talipes | |
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HP:0001945 | Fever | |
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HP:0002047 | Malignant hyperthermia | "Malignant hyperthermia is characterized by a rapid increase in temperature to 39-42 degrees C in response to inhalational anesthetics such as halothane or to muscle relaxants such as succinylcholine." [HPO:curators] |
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HP:0002167 | Neurological speech impairment | |
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HP:0002365 | Hypoplasia of the brainstem | |
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HP:0002650 | Scoliosis | "The presence of an abnormal lateral curvature of the spine." [HPO:curators] |
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HP:0002751 | Kyphoscoliosis | |
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HP:0002804 | Arthrogryposis multiplex congenita | |
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HP:0002827 | Dislocated hips | |
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HP:0002937 | Hemivertebrae | |
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HP:0002948 | Vertebral fusion | "A developmental defect leading to the union of two adjacent vertebrae." [HPO:curators] |
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HP:0002987 | Elbow contractures | |
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HP:0003044 | Shoulder contractures | |
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HP:0003049 | Ulnar deviation of the wrist | |
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HP:0003196 | Nasal hypoplasia | "Underdevelopment of the `nose` (FMA:46472)." [HPO:probinson] |
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HP:0003272 | Abnormality of the hip | "An abnormality of the hip joint or the surrounding anatomic region." [HPO:curators] |
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HP:0003273 | Hip contractures | |
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HP:0003298 | Spina bifida occulta | "The closed form of spina bifida." [HPO:curators] |
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HP:0003302 | Spondylolisthesis | |
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HP:0003422 | Vertebral segmentation defects | |
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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] |
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HP:0005272 | Prominent nasolabial folds | |
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HP:0005684 | Distal arthrogryposis | |
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HP:0005830 | Partial flexion contractures of fingers and toes | |
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HP:0006109 | Aplasia of the interphalangeal creases | "Absence of the interphalangeal creases of the fingers." [HPO:curators] |
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HP:0006380 | Knee flexion deformities | |
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HP:0006501 | Aplasia/Hypoplasia of the radius | "A small/hypoplastic or absent/aplastic radius." [HPO:curators] |
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HP:0006958 | Abnormal auditory evoked potentials | "An abnormality of the auditory evoked potentials, which are used to trace the signal generated by a sound, from the cochlear nerve, through the lateral lemniscus, to the medial geniculate nucleus, and to the cortex." [HPO:curators] |
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HP:0007598 | Bilateral single palmar creases | |
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HP:0008368 | Synostosis involving tarsal bones | |
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HP:0008872 | Feeding problems in infancy | |
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HP:0008897 | Growth retardation, progressive | |
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HP:0009465 | Ulnar deviation of fingers | |
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HP:0009473 | Joint contractures involving the joints of the hand | |
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HP:0010489 | Aplasia of the palmar creases | "Absence of the palmar creases." [HPO:curators] |
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HP:0010557 | Overlapping fingers | "Overlapping of the fingers occuring as the result of a deviation of the fingers from their normal position." [HPO:curators] |
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HP:0010751 | Chin dimple | "A persistent midline depression of the skin over the fat pad of the chin." [pmid:19125436] |
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HP:0011220 | Prominent forehead | "Forward prominence of the entire forehead, due to protrusion of the frontal bone." [pmid:19125436] |
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HP:0011824 | Chin with H-shaped crease | "H-shaped crease in the fat pad of the chin." [pmid:19125436] |
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HP:0012368 | Flat face | "Absence of concavity or convexity of the face when viewed in profile." [pmid:19125436] |
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HP:0012385 | Camptodactyly | "The distal interphalangeal joint and/or the proximal interphalangeal joint of the fingers or toes cannot be extended to 180 degrees by either active or passive extension." [HPO:probinson] |
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HP:0100490 | Camptodactyly (hands) | "Contractures of one ore more joints of the fingers." [HPO:sdoelken] |
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HP:0100790 | Hernia | |
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HP:0100830 | Round ear | |
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