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Tunnused
Geeniga IFT27 seotud tunnused
intraflagellar transport 27
Inimese fenotüübi ontoloogia seostab geeniga IFT27 113 tunnust kehasüsteemide kaupa: omadusi, mida täheldatakse inimestel, kellel on selle geeni üks haruldastest seisunditest.
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Abnormality of the genitourinary system
| Tunnus | Kui sageli seda täheldatakse |
|---|---|
| Abnormality of the genitourinary system | Sageli (30–79%) |
| Chronic kidney disease | Sageli (30–79%) |
| Underdeveloped ovary | Sageli (30–79%) |
| Underdeveloped penis | Sageli (30–79%) |
| Absent/small vagina | Mõnikord (5–29%) |
| Decreased testicular size | Mõnikord (5–29%) |
| Horseshoe kidney | Mõnikord (5–29%) |
| Hydrometrocolpos | Mõnikord (5–29%) |
| Hydronephrosis | Mõnikord (5–29%) |
| Infertility | Mõnikord (5–29%) |
| Lack of bladder control due to nervous system injury | Mõnikord (5–29%) |
| Menstrual irregularity | Mõnikord (5–29%) |
| Multiple kidney cysts | Mõnikord (5–29%) |
| Nephrotic syndrome | Mõnikord (5–29%) |
| Polycystic ovaries | Mõnikord (5–29%) |
| Renal failure | Mõnikord (5–29%) |
| Small kidneys | Mõnikord (5–29%) |
| Undescended testes | Mõnikord (5–29%) |
| Vesicoureteral reflux | Mõnikord (5–29%) |
| Underdevelopment of external reproductive organs | Pole registreeritud |
Abnormality of the nervous system
| Tunnus | Kui sageli seda täheldatakse |
|---|---|
| Delayed ability to walk | Alati |
| Delayed speech and language development | Alati |
| Global developmental delay | Alati |
| Underdevelopment of part of brain called corpus callosum | Alati |
| Neurodevelopmental delay | Väga sageli (80–99%) |
| Autism | Sageli (30–79%) |
| Behavioral abnormality | Sageli (30–79%) |
| Cognitive impairment | Sageli (30–79%) |
| Depression | Sageli (30–79%) |
| Short attention span | Sageli (30–79%) |
| Specific learning disability | Sageli (30–79%) |
| Abnormal speech pattern | Mõnikord (5–29%) |
| Anxiety | Mõnikord (5–29%) |
| Ataxia | Mõnikord (5–29%) |
| Breathy speech | Mõnikord (5–29%) |
| Can't control feelings | Mõnikord (5–29%) |
| Epilepsy | Mõnikord (5–29%) |
| Intellectual disability | Mõnikord (5–29%) |
Abnormality of the eye
| Tunnus | Kui sageli seda täheldatakse |
|---|---|
| Breakdown of light-sensitive cells in back of eye | Alati |
| Close sighted | Alati |
| Cone/cone-rod dystrophy | Alati |
| Exodeviation | Alati |
| Rod-cone dystrophy | Alati |
| Abnormal color vision | Sageli (30–79%) |
| Abnormal electroretinogram | Sageli (30–79%) |
| Blindness | Sageli (30–79%) |
| Decreased clarity of vision | Sageli (30–79%) |
| Difficulties with night vision | Sageli (30–79%) |
| Extreme sensitivity of the eyes to light | Sageli (30–79%) |
| Involuntary, rapid, rhythmic eye movements | Sageli (30–79%) |
| Astigmatism | Mõnikord (5–29%) |
| Clouding of the lens of the eye | Mõnikord (5–29%) |
| Cross-eyed | Mõnikord (5–29%) |
| Wide-set eyes | Mõnikord (5–29%) |
Abnormality of head or neck
| Tunnus | Kui sageli seda täheldatakse |
|---|---|
| Abnormality of the oral cavity | Sageli (30–79%) |
| Abnormality of the sense of smell | Sageli (30–79%) |
| Dental crowding | Sageli (30–79%) |
| Failure of development of between one and six teeth | Sageli (30–79%) |
| High palate | Sageli (30–79%) |
| Decreased size of tooth | Mõnikord (5–29%) |
| Depressed nasal bridge | Mõnikord (5–29%) |
| Downward slanting of the opening between the eyelids | Mõnikord (5–29%) |
| Long philtrum | Mõnikord (5–29%) |
| Medial flaring of the eyebrow | Mõnikord (5–29%) |
| Nasal inflammation | Mõnikord (5–29%) |
| Prominent nasal bridge | Mõnikord (5–29%) |
| Receding chin | Mõnikord (5–29%) |
| Short neck | Mõnikord (5–29%) |
| Hyposmia | Pole registreeritud |
Abnormality of limbs
| Tunnus | Kui sageli seda täheldatakse |
|---|---|
| Extra toe attached near the little toe | Alati |
| Mesoaxial hand polydactyly | Alati |
| Y-shaped long bone of hand | Alati |
| Postaxial polydactyly | Väga sageli (80–99%) |
| Short fingers or toes | Sageli (30–79%) |
| Club feet | Mõnikord (5–29%) |
| Finger syndactyly | Mõnikord (5–29%) |
| Webbed fingers or toes | Mõnikord (5–29%) |
| Curvature of outermost bone of little finger | Harva (1–4%) |
Abnormality of the cardiovascular system
| Tunnus | Kui sageli seda täheldatakse |
|---|---|
| Partial atrioventricular canal defect | Alati |
| High blood pressure | Sageli (30–79%) |
| Abnormality of the heart | Mõnikord (5–29%) |
| An opening in the wall separating the top two chambers of the heart | Mõnikord (5–29%) |
| Hole in heart wall separating two lower heart chambers | Mõnikord (5–29%) |
| Patent ductus arteriosus | Mõnikord (5–29%) |
| Underdeveloped left heart | Mõnikord (5–29%) |
| Disease of the heart muscle | Harva (1–4%) |
Laboratory abnormality
| Tunnus | Kui sageli seda täheldatakse |
|---|---|
| Decreased circulating high-density lipoprotein cholesterol | Sageli (30–79%) |
| High liver enzymes | Sageli (30–79%) |
| Impaired fasting glucose | Sageli (30–79%) |
| Increased plasma triglycerides | Sageli (30–79%) |
| Body fails to respond to insulin | Mõnikord (5–29%) |
| Fatty infiltration of liver | Mõnikord (5–29%) |
| Noninsulin-dependent diabetes | Mõnikord (5–29%) |
Abnormality of the digestive system
| Tunnus | Kui sageli seda täheldatakse |
|---|---|
| Abnormality of the gastrointestinal tract | Mõnikord (5–29%) |
| Hepatic fibrosis | Mõnikord (5–29%) |
| Celiac disease | Harva (1–4%) |
| Enlarged colon lacking nerve cells | Harva (1–4%) |
| Inflammation of the large intestine | Harva (1–4%) |
Abnormality of the ear
| Tunnus | Kui sageli seda täheldatakse |
|---|---|
| Ears rotated toward back of head | Mõnikord (5–29%) |
| Hearing impairment | Mõnikord (5–29%) |
| Large ears | Mõnikord (5–29%) |
| Middle ear infection | Mõnikord (5–29%) |
Abnormality of the endocrine system
| Tunnus | Kui sageli seda täheldatakse |
|---|---|
| Decreased activity of gonads | Sageli (30–79%) |
| Abnormality of the endocrine system | Mõnikord (5–29%) |
| Underactive thyroid | Mõnikord (5–29%) |
Abnormality of the musculoskeletal system
| Tunnus | Kui sageli seda täheldatakse |
|---|---|
| Double-Jointed | Mõnikord (5–29%) |
| Involuntary muscle stiffness, contraction, or spasm | Mõnikord (5–29%) |
| Muscle degeneration | Mõnikord (5–29%) |
Growth abnormality
| Tunnus | Kui sageli seda täheldatakse |
|---|---|
| Obesity | Alati |
| Childhood-onset truncal obesity | Väga sageli (80–99%) |
| Short stature | Sageli (30–79%) |
Abnormality of the immune system
| Tunnus | Kui sageli seda täheldatakse |
|---|---|
| Asthma | Mõnikord (5–29%) |
Abnormality of the integument
| Tunnus | Kui sageli seda täheldatakse |
|---|---|
| Excessive hairiness over body | Mõnikord (5–29%) |
Kui sageli see esineb geenist tulenevate seisunditega inimeste seas, kõige sagedamini nende kõigi seas, nagu on märgitud Inimese fenotüübi ontoloogias. Need lehed kirjeldavad tunnuseid ja nende taga olevaid uuringuid; need ei ole diagnoos ning sümptomite kohta tuleks küsida arstilt või geneetilt nõustajalt.
Allikas
- Inimese fenotüübi ontoloogia, versioon 2026-09-01: geeniga IFT27 seotud tunnused ja iga tunnuse esinemissagedus. Lisateavet leiate aadressilt hpo.jax.org.
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