「RECESSIVE」の共起表現一覧(1語右で並び替え)
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| Since the gene is | recessive, all offspring will be heterozygous, and the |
| esistance to Bt will evolve in the form of a | recessive allele in the pest. |
| helytoky phenotype, which is controlled by a | recessive allele at a single locus (workers must be ho |
| Hardy-Weinberg proportions, with r' 1 for a | recessive allele and r' 1 for a codominant or dominant |
| White lions owe their coloring to a | recessive allele. |
| fspring if both parents were carriers of the | recessive allele. |
| rent mutations lead to dominant-negative and | recessive alleles. |
| Both are autosomal | recessive and affect males and females equally. |
| this disease: Autosomal dominant, autosomal | recessive and de novo. |
| y inheritance (autosomal dominant, autosomal | recessive, and X-linked) or by which structures are in |
| I/NIH/UW entry on CARASIL Cerebral Autosomal | Recessive Arteriopathy with Subcortical Infarcts and L |
| emia, is a rare, relatively benign autosomal | recessive bilirubin disorder of unknown origin. |
| or lionitis) is an extremely rare autosomal | recessive bone disorder that causes calcium to build u |
| Inheritance is thought to be autosomal | recessive, but this cannot be established as individua |
| is usually autosomal dominant, though a few | recessive cases have been noted. |
| al dominant manner, although a few autosomal | recessive cases have been noted. |
| X-linked | recessive chondrodysplasia punctata is a type of chond |
| X-linked | recessive chondrodysplasia punctata 302950 |
| tion, if it is a naturally occurring, albeit | recessive, color, an albino characteristic, or an unhe |
| chner-Hanhart syndrome":543) is an autosomal | recessive condition with onset between ages 2 and 4 ye |
| ion or Batten Mayou syndrome is an autosomal | recessive condition which commences in the first decad |
| congenital lipodystrophy is a rare autosomal | recessive condition associating insulin resistance, ab |
| It is an autosomal | recessive condition and is one of the few disorders of |
| X-linked | recessive conditions include the serious diseases Hemo |
| ma with digital changes, is a rare autosomal | recessive congenital disorder first reported in 1939 b |
| Neill-Dingwall Syndrome) is a rare autosomal | recessive congenital disorder characterized by growth |
| absent corpus callosum, is a rare autosomal | recessive congenital disorder characterized by albinis |
| botten type") is an extremely rare autosomal | recessive congenital skin disorder in which dry, thick |
| heriff Phillips syndrome is a rare autosomal | recessive congenital disorder. |
| MORM syndrome is an autosomal | recessive congenital disorder characterized by mental |
| e have been documented in cases of autosomal | recessive congenital alopecia and atrichia with papula |
| ght-Hodes syndrome, is a very rare autosomal | recessive congenital disorder. |
| It is an autosomal | recessive congenital skin disease characterized by a c |
| Fountain syndrome is an autosomal | recessive congenital disorder characterized by mental |
| peculiar facial expression, is an autosomal | recessive congenital disorder characterized by inverte |
| oculocerebrofacial syndrome is an autosomal | recessive congenital disorder characterized by mental |
| Macular dystrophy syndrome) is an autosomal | recessive congenital malformation disorder affecting t |
| and Seemanova syndrome, is a rare autosomal | recessive congenital disorder causing chromosomal inst |
| s syndrome, is a rare, very severe autosomal | recessive congenital disorder characterized by malform |
| y of excinuclease occurs in a rare autosomal | recessive disease called xeroderma pigmentosum. |
| e the cause of pycnodysostosis, an autosomal | recessive disease characterized by osteosclerosis and |
| iciency and agammaglobulinemia, an autosomal | recessive disease in which few or no gamma globulins o |
| It is an autosomal | recessive disease and is likely due to a loss of funct |
| Hypophosphatasia, an autosomal | recessive disease |
| It is classified as an autosomal | recessive disease, one that can be passed down through |
| sia (CAH) refers to any of several autosomal | recessive diseases resulting from defects in steps of |
| A woman who is a carrier of an X-linked | recessive disorder (XRXr) has a 50% chance of having s |
| It is a rare, ciliopathic, autosomal | recessive disorder characterized by nephronophthisis a |
| Trimethylaminuria is an autosomal | recessive disorder involving a trimethylamine oxidase |
| e transcarbamylase deficiency is an X-linked | recessive disorder caused by a number of different mut |
| It is an autosomal | recessive disorder in which mild clinical manifestatio |
| The parents of a child with an autosomal | recessive disorder are carriers of one copy of the def |
| Aceruloplasminemia is an autosomal | recessive disorder of iron metabolism characterized by |
| nown as Pompe disease, which is an autosomal | recessive disorder with a broad clinical spectrum. |
| ult progeria":573) is a very rare, autosomal | recessive disorder characterized by the appearance of |
| n-responsive basal ganglia disease (BBGD); a | recessive disorder manifested in childhood that progre |
| eshift mutations in this gene lead to a rare | recessive disorder characterised by severe failure to |
| patic lipase deficiency is a rare, autosomal | recessive disorder that results in elevated high densi |
| type 2 (HPLH2), a rare and lethal autosomal | recessive disorder of early childhood. |
| e parents of an individual with an autosomal | recessive disorder each carry one copy of the altered |
| e parents of an individual with an autosomal | recessive disorder both carry one copy of the defectiv |
| nemia syndrome (TRMA), which is an autosomal | recessive disorder characterized by diabetes mellitus, |
| Dubin-Johnson syndrome is an autosomal | recessive disorder that causes an increase of conjugat |
| se of Papillon-Lefevre disease, an autosomal | recessive disorder characterized by palmoplantar kerat |
| e parents of an individual with an autosomal | recessive disorder both carry one copy of the defectiv |
| e parents of an individual with an autosomal | recessive disorder are carriers of one copy of the alt |
| It is an autosomal | recessive disorder that results from inappropriately l |
| ry carnitine deficiency (CDSP), an autosomal | recessive disorder manifested early in life by hypoket |
| e parents of an individual with an autosomal | recessive disorder are carriers of one copy of the alt |
| immunoosseous dysplasia (SIOD), an autosomal | recessive disorder with the diagnostic features of spo |
| "Chanarin-Dorfman syndrome") is an autosomal | recessive disorder characterized by accumulation of tr |
| eijadinhos (Brazilian type), is an autosomal | recessive disorder that results in hemimelia, a lack o |
| Refsum disease, an autosomal | recessive disorder that results from the accumulation |
| e parents of an individual with an autosomal | recessive disorder are carriers of one copy of the def |
| e parents of an individual with an autosomal | recessive disorder each carry one copy of the defectiv |
| I-cell disease is an autosomal | recessive disorder caused by a deficiency of GlcNAc ph |
| e parents of an individual with an autosomal | recessive disorder each carry one copy of the altered |
| It is an autosomal | recessive disorder, which means the defective gene res |
| Cystinuria is an autosomal | recessive disorder, which means that the defective gen |
| Although it is an autosomal | recessive disorder, heterozygotes may still manifest m |
| ea-acanthocytosis is considered an autosomal | recessive disorder, although a few cases with autosoma |
| EEM syndrome is an autosomal | recessive disorder, which means the defective gene is |
| e is thought to be inherited as an autosomal | recessive disorder. |
| for a person to be affected by an autosomal | recessive disorder. |
| It is an autosomal | recessive disorder. |
| There are five typical autosomal | recessive disorders in which ataxia is a prominent fea |
| Males are affected by X-linked | recessive disorders much more frequently than females. |
| herefore feel that the lists of dominant and | recessive disorders (limited to humans at that) are no |
| Three autosomal | recessive disorders involve the inability to metaboliz |
| There are five typical autosomal | recessive disorders in which ataxia is a prominent fea |
| nant disorders" and "List if human autosomal | recessive disorders". |
| ption of melanin synthesis and all autosomal | recessive disorders.:864 |
| They may be inherited in a | recessive, dominant, or X-linked manner, depending on |
| ique features of ancon sheep are caused by a | recessive dwarf mutation, which often results in cripp |
| Diastrophic dysplasia (DTD) is an autosomal | recessive dysplasia which affects cartilage and bone d |
| Mutations in emerin cause X-linked | recessive Emery-Dreifuss muscular dystrophy. |
| pe 2, this syndrome inherits in an autosomal | recessive fashion and is due to a defect in AIRE ("aut |
| earwax, are also determined in an autosomal | recessive fashion. |
| utaneous condition inherited in an autosomal | recessive fashion. |
| unctional protein deficiency is an autosomal | recessive fatty acid oxidation disorder that prevents |
| iciency and SCAD deficiency, is an autosomal | recessive fatty acid oxidation disorder which affects |
| tology to X-SCID in humans, and an autosomal | recessive form seen in one line of Jack Russell Terrie |
| The autosomal | recessive form of SCID has been identified in one line |
| lled cerebral cholesterosis, is an autosomal | recessive form of xanthomatosis. |
| type 1 or Oguchi disease 1, is an autosomal | recessive form of congenital stationary night blindnes |
| Adducted thumb syndrome | recessive form, also known as Christian syndrome or Cr |
| Autosomal | recessive forms |
| nesis was found to be the most common of the | recessive forms of osteochondrodysplasia, with a preva |
| evolutionary change of the frequency of the | recessive gene |
| q is the frequency of the | recessive gene |
| suggests that being white is the result of a | recessive gene, and that racism is a white survival in |
| o forms of inherited human muscle disorders: | recessive generalized myotonia congenita (Becker) and |
| lly a black Oberhasli appears as a result of | recessive genes. |
| phocyte syndrome, type II (BLS II) is a rare | recessive genetic condition in which a group of genes |
| secondary hypocalcemia (HSH) is an autosomal | recessive genetic disorder affecting intestinal magnes |
| e is thought to be inherited as an autosomal | recessive genetic trait. |
| sity of the mutation base for many autosomal | recessive genetic disorders. |
| Behr syndrome is an autosomal | recessive genetic disorder named after Carl Behr, who |
| as "Small eye", believed to be an autosomal | recessive genetic condition. |
| yndrome (AMS) is an extremely rare autosomal | recessive genetic disorder characterized by malformati |
| hate dehydrogenase deficiency is an X-linked | recessive genetic disease. |
| or horn cell disease (LAAHD) is an autosomal | recessive genetic disorder characterized by reduced mo |
| Kapur-Toriello syndrome is a rare autosomal | recessive genetic disorder, characterised by severe me |
| Keutel syndrome is a rare autosomal | recessive genetic disorder characterized by abnormal d |
| ect in xeroderma pigmentosum is an autosomal | recessive genetic defect in which nucleotide excision |
| ture syndrome, Finnish type, is an autosomal | recessive genetic disorder characterized by total immo |
| GAPO syndrome is a rare, autosomal | recessive genetic disorder. |
| Kindler syndrome is an autosomal | recessive genodermatosis. |
| ygous dominant, heterozygous, and homozygous | recessive genotypes respectively. |
| this gene has been associated with autosomal | recessive HEM/Greenberg skeletal dysplasia. |
| This deficiency, an X-linked | recessive hereditary disease, is the most common enzym |
| lycosylase, causing a rare form of autosomal | recessive Hyper IgM syndrome, and on STAT3, the gene c |
| Patients with autosomal | recessive hypercholesterolemia tend to have more sever |
| trait with variable expressivity but can be | recessive if the associated osteogenesis imperfecta is |
| anomalies syndrome) is a very rare autosomal | recessive immune disorder. |
| iseases can be inherited two ways: Autosomal | recessive inheritance occurs when both parents carry a |
| Both autosomal dominant and | recessive inheritance have been observed with the diso |
| Both autosomal dominant and | recessive inheritance have been reported with the diso |
| Autosomal | recessive inheritance means two copies of the gene in |
| The difference between dominant and | recessive inheritance patterns also plays a role in de |
| The disorder has an autosomal | recessive inheritance pattern, which means the defecti |
| Urocanic aciduria has an autosomal | recessive inheritance pattern, which means the defecti |
| Autosomal | recessive inheritance means the defective gene respons |
| It exhibits autosomal | recessive inheritance, and the responsible gene is loc |
| as cousins), often associated with autosomal | recessive inheritance, has been attributed to the inhe |
| a poorly characterized disorder, probably of | recessive inheritance, that includes epilepsy, mental |
| nd Factor cannot bind Factor VIII, autosomal | recessive inheritance. |
| isease, is metabolic disorder with autosomal | recessive inheritance. |
| parents, giving the possibility of autosomal | recessive inheritance. |
| X-linked | recessive inheritance. |
| It is of autosomal | recessive inheritance. |
| Aase syndrome is thought to be an autosomal | recessive inherited disorder. |
| CHH is an autosomal | recessive inherited disorder. |
| Because Wolman disease is autosomal | recessive, it is expected to occur at higher frequenci |
| Meckel-Gruber syndrome (MKS) is an autosomal | recessive lethal malformation. |
| Recessive lethal alleles don't cause death in the hete | |
| If the mutation is caused by a | recessive lethal allele, the homozygote for the allele |
| roduced to a germline of mice, they caused a | recessive lethal phenotype. |
| Three different | recessive, loss of function mutations in the encoded p |
| matosis":545) is an extremely rare autosomal | recessive lysosomal storage disease that cause an accu |
| t is believed to be inherited in an X-linked | recessive manner, which means a genetic mutation causi |
| stmann syndrome is inherited in an autosomal | recessive manner, but may occasionally be autosomal do |
| mucolipidoses are inherited in an autosomal | recessive manner, that is, they occur only when a chil |
| The disease is inherited in an autosomal | recessive manner. |
| LCCS1 is inherited in an autosomal | recessive manner. |
| Hyperlysinemia is inherited in an autosomal | recessive manner. |
| Nakajo syndrome is inherited in an autosomal | recessive manner. |
| is believed to be inherited in an autosomal | recessive manner. |
| gested that AMS is inherited in an autosomal | recessive manner. |
| defect is usually inherited in an autosomal | recessive manner. |
| in either an autosomal dominant or autosomal | recessive manner. |
| inherited in either an autosomal dominant or | recessive manner. |
| The disorder is inherited in an autosomal | recessive manner. |
| tase deficiency is inherited in an autosomal | recessive manner. |
| ystathioninuria is inherited in an autosomal | recessive manner. |
| This syndrome is inherited in an autosomal | recessive manner. |
| CAMFAK syndrome is inherited in an autosomal | recessive manner. |
| Rotor syndrome is inherited in an autosomal | recessive manner. |
| It is inherited in an autosomal | recessive manner. |
| RL syndrome is inherited in an autosomal | recessive manner. |
| APRT deficiency is inherited in an autosomal | recessive manner. |
| GAPO syndrome is inherited in an autosomal | recessive manner. |
| Lucey-Driscoll syndrome is an autosomal | recessive metabolic disorder affecting enzymes involve |
| lled methylmalonic aciduria, is an autosomal | recessive metabolic disorder. |
| It is a rare, autosomal | recessive metabolic disorder affecting heme, caused by |
| Blue diaper syndrome is a rare, autosomal | recessive metabolic disorder characterized in infants |
| eficiency (CPS I deficiency) is an autosomal | recessive metabolic disorder that causes ammonia to ac |
| translocase deficiency is a rare, autosomal | recessive metabolic disorder that prevents the body fr |
| Sandhoff disease is a rare, autosomal | recessive metabolic disorder that causes progressive d |
| rred to as histidinuria, is a rare autosomal | recessive metabolic disorder caused by a deficiency of |
| gliosidosis, AB variant is a rare, autosomal | recessive metabolic disorder that causes progressive d |
| ed cystathionase deficiency, is an autosomal | recessive metabolic disorder that results in an excess |
| hydroxyadenine urolithiasis) is an autosomal | recessive metabolic disorder associated with a mutatio |
| also called GAMT deficiency, is an autosomal | recessive metabolic disorder that primarily affects th |
| o called mevalonic aciduria, is an autosomal | recessive metabolic disorder that disrupts the biosynt |
| ncy or urocanase deficiency, is an autosomal | recessive metabolic disorder caused by a deficiency of |
| Cystinuria is an inherited autosomal | recessive metabolic disorder that is characterized by |
| Glutaric acidemia type 2 is an autosomal | recessive metabolic disorder that is characterised by |
| Hyperlysinemia is an autosomal | recessive metabolic disorder characterized by an abnor |
| ia and SARDH deficiency, is a rare autosomal | recessive metabolic disorder characterized by an incre |
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