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Požymiai
Su BBS10 susiję požymiai
Bardet-Biedl syndrome 10
Žmogaus fenotipo ontologija sieja 100 požymių su BBS10, pagal kūno sistemas: požymiai, pastebimi žmonėms, sergantiems viena iš šio geno retųjų ligų.
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PrisijungtiKlaustiSekvenuokite savo genomą↗
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PrisijungtiKlaustiSekvenuokite savo genomą↗
Abnormality of the genitourinary system
| Požymis | Kaip dažnai pasireiškia |
|---|---|
| Abnormality of the genitourinary system | Dažnai (30–79%) |
| Chronic kidney disease | Dažnai (30–79%) |
| Underdeveloped ovary | Dažnai (30–79%) |
| Underdeveloped penis | Dažnai (30–79%) |
| Absent/small vagina | Kartais (5–29%) |
| Decreased testicular size | Kartais (5–29%) |
| Horseshoe kidney | Kartais (5–29%) |
| Hydrometrocolpos | Kartais (5–29%) |
| Hydronephrosis | Kartais (5–29%) |
| Infertility | Kartais (5–29%) |
| Lack of bladder control due to nervous system injury | Kartais (5–29%) |
| Menstrual irregularity | Kartais (5–29%) |
| Multiple kidney cysts | Kartais (5–29%) |
| Nephrotic syndrome | Kartais (5–29%) |
| Polycystic ovaries | Kartais (5–29%) |
| Undescended testes | Kartais (5–29%) |
| Vesicoureteral reflux | Kartais (5–29%) |
| Cystic kidney disease | Neužfiksuota |
| Renal failure | Neužfiksuota |
Abnormality of the nervous system
| Požymis | Kaip dažnai pasireiškia |
|---|---|
| Epilepsy | Visada |
| Global developmental delay | Visada |
| Intellectual disability, mild | Visada |
| Neurodevelopmental delay | Labai dažnai (80–99%) |
| Autism | Dažnai (30–79%) |
| Behavioral abnormality | Dažnai (30–79%) |
| Cognitive impairment | Dažnai (30–79%) |
| Depression | Dažnai (30–79%) |
| Short attention span | Dažnai (30–79%) |
| Specific learning disability | Dažnai (30–79%) |
| Abnormal speech pattern | Kartais (5–29%) |
| Anxiety | Kartais (5–29%) |
| Ataxia | Kartais (5–29%) |
| Breathy speech | Kartais (5–29%) |
| Can't control feelings | Kartais (5–29%) |
| Delayed speech and language development | Kartais (5–29%) |
| Intellectual disability | Kartais (5–29%) |
Abnormality of head or neck
| Požymis | Kaip dažnai pasireiškia |
|---|---|
| Abnormality of the oral cavity | Dažnai (30–79%) |
| Abnormality of the sense of smell | Dažnai (30–79%) |
| Dental crowding | Dažnai (30–79%) |
| Failure of development of between one and six teeth | Dažnai (30–79%) |
| High palate | Dažnai (30–79%) |
| Decreased size of tooth | Kartais (5–29%) |
| Depressed nasal bridge | Kartais (5–29%) |
| Downward slanting of the opening between the eyelids | Kartais (5–29%) |
| Long philtrum | Kartais (5–29%) |
| Medial flaring of the eyebrow | Kartais (5–29%) |
| Nasal inflammation | Kartais (5–29%) |
| Prominent nasal bridge | Kartais (5–29%) |
| Receding chin | Kartais (5–29%) |
| Short neck | Kartais (5–29%) |
Abnormality of the eye
| Požymis | Kaip dažnai pasireiškia |
|---|---|
| Breakdown of light-sensitive cells in back of eye | Visada |
| Rod-cone dystrophy | Visada |
| Cone/cone-rod dystrophy | Labai dažnai (80–99%) |
| Abnormal color vision | Dažnai (30–79%) |
| Abnormal electroretinogram | Dažnai (30–79%) |
| Blindness | Dažnai (30–79%) |
| Decreased clarity of vision | Dažnai (30–79%) |
| Difficulties with night vision | Dažnai (30–79%) |
| Extreme sensitivity of the eyes to light | Dažnai (30–79%) |
| Involuntary, rapid, rhythmic eye movements | Dažnai (30–79%) |
| Astigmatism | Kartais (5–29%) |
| Clouding of the lens of the eye | Kartais (5–29%) |
| Cross-eyed | Kartais (5–29%) |
| Wide-set eyes | Kartais (5–29%) |
Laboratory abnormality
| Požymis | Kaip dažnai pasireiškia |
|---|---|
| Decreased circulating high-density lipoprotein cholesterol | Dažnai (30–79%) |
| High liver enzymes | Dažnai (30–79%) |
| Impaired fasting glucose | Dažnai (30–79%) |
| Increased plasma triglycerides | Dažnai (30–79%) |
| Body fails to respond to insulin | Kartais (5–29%) |
| Fatty infiltration of liver | Kartais (5–29%) |
| Noninsulin-dependent diabetes | Kartais (5–29%) |
Abnormality of limbs
| Požymis | Kaip dažnai pasireiškia |
|---|---|
| Postaxial polydactyly | Dažnai (30–79%) |
| Short fingers or toes | Dažnai (30–79%) |
| Club feet | Kartais (5–29%) |
| Finger syndactyly | Kartais (5–29%) |
| Webbed fingers or toes | Kartais (5–29%) |
| Curvature of outermost bone of little finger | Retai (1–4 %) |
Abnormality of the digestive system
| Požymis | Kaip dažnai pasireiškia |
|---|---|
| Abnormality of the gastrointestinal tract | Kartais (5–29%) |
| Hepatic fibrosis | Kartais (5–29%) |
| Celiac disease | Retai (1–4 %) |
| Enlarged colon lacking nerve cells | Retai (1–4 %) |
| Inflammation of the large intestine | Retai (1–4 %) |
Abnormality of the ear
| Požymis | Kaip dažnai pasireiškia |
|---|---|
| Ears rotated toward back of head | Kartais (5–29%) |
| Hearing impairment | Kartais (5–29%) |
| Large ears | Kartais (5–29%) |
| Middle ear infection | Kartais (5–29%) |
Abnormality of the cardiovascular system
| Požymis | Kaip dažnai pasireiškia |
|---|---|
| High blood pressure | Dažnai (30–79%) |
| Abnormality of the heart | Kartais (5–29%) |
| Disease of the heart muscle | Retai (1–4 %) |
Abnormality of the endocrine system
| Požymis | Kaip dažnai pasireiškia |
|---|---|
| Decreased activity of gonads | Dažnai (30–79%) |
| Abnormality of the endocrine system | Kartais (5–29%) |
| Underactive thyroid | Kartais (5–29%) |
Abnormality of the musculoskeletal system
| Požymis | Kaip dažnai pasireiškia |
|---|---|
| Double-Jointed | Kartais (5–29%) |
| Involuntary muscle stiffness, contraction, or spasm | Kartais (5–29%) |
| Muscle degeneration | Kartais (5–29%) |
Growth abnormality
| Požymis | Kaip dažnai pasireiškia |
|---|---|
| Obesity | Visada |
| Childhood-onset truncal obesity | Labai dažnai (80–99%) |
| Short stature | Dažnai (30–79%) |
Abnormality of the immune system
| Požymis | Kaip dažnai pasireiškia |
|---|---|
| Asthma | Kartais (5–29%) |
Abnormality of the integument
| Požymis | Kaip dažnai pasireiškia |
|---|---|
| Excessive hairiness over body | Kartais (5–29%) |
Kaip dažnai šis požymis pasitaiko žmonėms, turintiems vieną iš geno sukeliamų ligų, ir kuris dažnis tarp jų didžiausias, pagal Žmogaus fenotipo ontologijos duomenis. Šiuose puslapiuose aprašomi požymiai ir juos grindžiantys tyrimai; tai nėra diagnozė, o su simptomais kreipkitės į gydytoją ar genetikos konsultantą.
Iš kur tai žinoma
- Žmogaus fenotipo ontologija, 2026-09-01 leidimas: su BBS10 susiję požymiai ir kaip dažnai kiekvienas pasitaiko. Daugiau informacijos rasite adresu hpo.jax.org.
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PrisijungtiKlaustiSekvenuokite savo genomą↗
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