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Results for A in English, page 202
allantoinase activity
Allantoinase protein, S cerevisiae
Allantoine
Allantoine [Moles/time] in 24 hour Urine by Electrophoresis
Allantoine [Moles/volume] in Urine
Allantoine | Urine
Allantoine 24H Ur Elph-sRate
allantoine amidinohydrolase activity
Allantoine Ur-sCnc
Allantoine:SCnc:Pt:Urine:Qn
Allantoine:SRat:24H:Urine:Qn:Electrophoresis
Allantoine:Substance Concentration:Point in time:Urine:Quantitative
Allantoine:Substance Rate:24 hours:Urine:Quantitative:Electrophoresis
Allantois
allantoises
Allantoma
Allantoma lineata
Allantoma lineata (Mart. & O.Berg) Miers
Allantoma Miers
Allantonematidae
Allantoparmelia
Allantoparmelia alpicola
Allantophoma
Allantophoma endogenospora
Allantophomopsis
Allantophomopsis lycopodina
allantostatin I
allantoxanamide
Allantus
Allantus luctifer
Allantus luctifer (F. Smith, 1874)
allanxanthone B
allanxanthone C
allanxanthone E
Allanzyme
Allanzyme, 650,000 units/g-10% topical ointment
Allanzyme, 830,000 units/g-10% topical ointment
allapinin
allapinine
Allardia
Allardia Decne.
Allardia tomentosa
Allardia tomentosa Decne.
Allartedius corallinus
Allas
Allas diplophysa
Allas sp. (3108W2)
Allas sp. (SA)
Allas sp. JJP-2003
Allassogonoporus
Allassogonoporus amphoraeformis
Allata, Corpora
allatinhibin
allative case
allatohibin
Allatostatin
allatostatin 1
allatostatin A1
allatostatin A2
allatostatin activity
allatostatin B-type, Cancer borealis
allatostatin protein, Manduca sexta
Allatostatin Receptor 2 protein, Drosophila
allatostatin receptor activity
Allatostatin Receptor protein, Drosophila
allatostatin receptor, Drosophila
allatostatin receptor, mouse
allatostatin receptors, mouse
allatostatin-A1
allatostatin-A2
allatostatin, Diploptera puncta, juvenile hormone inhibitor
allatostatin, Manduca sexta
allatotropin
allatotropin (5-13), N-acetylVal-Nle(7,8)-
allatotropin (5-13), N-acetylvalyl-norleucine(7,8)-
allatotropin (5-13), Nle(7,8)-
allatotropin (5-13), norleucine (7,8)-
Allatum, Corpus
ALLAVGATK
Allay
Allay 5/500 (hydrocodone / acetaminophen) Oral Capsule
Allay gel
Allay, 500 mg-5 mg oral capsule
allayed
allaying
allays
Allbee with C
Allbee with Vitamin C
Allbee-C
Allbee-C 800
Allbee-C 800 with Iron
Allbee-C 800 with Iron, Vitamin B Complex with C and Iron oral tablet
Allbee-C 800, Vitamin B Complex with C oral tablet
Allbee-C, Vitamin B Complex with C oral tablet
ALLC
ALLC gene
AllCeram
ALLCLENZ
ALLCLENZ SPRAY,TOP
ALLCLENZ SPRAY,TOP [VA Product]
ALLCLENZ TOP SPRAY
Allclenz Wound Cleanser
Allcorr
Alldent Sinomer
alldimycin A
alldimycin B
alldimycin C
Alldress Dressing 4x4"
Alldress Dressing 6 x 6"
Alldress Dressing 6 x 8"
Alle
Alle alle
Alleculinae sp. UPOL ZL0030
Alleculinae sp. UPOL ZL0064
Alleculinae sp. UPOL ZL0065
Alleculinae sp. UPOL ZL0166
allegation
Allegation, False
allegations
Allegations have been made that ...
Allegations, False
allege
allegeable
alleged
allegedly
allegement
alleges
allegest
allegeth
Allegheny barberry
Allegheny blackberry
Allegheny plum
Allegheny-vine
allegiance
allegiances
alleging
allegorated
allegorating
allegoric
allegorical
allegorically
allegorised
allegorising
allegorized
allegorizes
allegorizing
allegory
Allegra
Allegra 120 MG Oral Tablet
Allegra 180 MG Oral Tablet
Allegra 30 MG Disintegrating Tablet
Allegra 30 MG Oral Tablet
Allegra 6 MG/ML Oral Suspension
Allegra 60 MG Oral Capsule
Allegra 60 MG Oral Tablet
Allegra ODT
Allegra ODT, 30 mg oral tablet, disintegrating
Allegra-D
Allegra-D 12 Hour
Allegra-D 12 Hour 60-120 MG Extended Release Tablet
Allegra-D 12 Hour, 60 mg-120 mg oral tablet, extended release
Allegra-D 24 Hour
Allegra-D 24 Hour 180-240 MG Extended Release Tablet
Allegra-D 24 Hour 180mg-240mg Extended-Release Tablet
Allegra-D 24 Hour, 180 mg-240 mg oral tablet, extended release
Allegra-D, 60 mg-120 mg oral tablet, extended release
Allegra, 180 mg oral tablet
Allegra, 30 mg oral tablet
Allegra, 30 mg/5 mL oral suspension
Allegra, 60 mg oral capsule
Allegra, 60 mg oral tablet
Allegro
allegro#allegro (Englisch)|allegro
Allegron
allegros
Allele
Allele Frequencies
Allele Frequency
Allele name
Allele name [Identifier] in Blood or Tissue by Molecular genetics method
Allele name Bld/T
Allele name:ID:Pt:Bld/Tiss:Nom:Molgen
Allele name:Identifier:Point in time:Whole blood/Tissue, unspecified:Nominal:MOLECULAR GENETICS
Allele_Absent_From_Wild-type_Chromosomal_Location
Allele_Associated_With_Disease
Allele_Ceases_Function_In_Pathway
Allele_Has_Abnormality
Allele_Has_Activity
Allele_In_Chromosomal_Location
Allele_Is_Cancer_Related_Type
Allele_Not_Associated_With_Abnormality
Allele_Not_Associated_With_Disease
Allele_Plays_Altered_Role_In_Process
Allele_Plays_Role_In_Metabolism_Of_Chemical_Or_Drug
Allele, Lethal
Allele, X-Linked
Allele, Y-Linked
Alleles
Alleles, Lethal
Alleles, X Linked
Alleles, X-Linked
Alleles, Y Linked
Alleles, Y-Linked
Allelic corneal dystrophy Groenow type ({121900}), Thiel-Behnke type ({602082}), lattice type I ({122200}), Avellino type ({607541}), Reis-Bucklers type ({608470}) and epithelial basement membrane ({121820})
Allelic disorder is Brugada syndrome ({601144})
Allelic disorder is long QT syndrome-3 (LQT3, {603830})
Allelic disorder to a form of dilated cardiomyopathy (CMD1G, {604145})
Allelic disorder to adult polyglucosan body disease ({263570})
Allelic disorder to androgen insensitivity syndrome (AIS, {300068})
Allelic disorder to ankyloblepharon-ectodermal defects, cleft lip/palate syndrome (AEC, {106260})
Allelic disorder to autosomal dominant form ({129490})
Allelic disorder to autosomal dominant nonsyndromic sensorineural deafness (DFNA11, {601317}) and Usher syndrome type IB ({276900})
Allelic disorder to autosomal dominant optic atrophy and cataract ({165300})
Allelic disorder to autosomal dominant SPG13 ({605280})
Allelic disorder to autosomal recessive deafness 21 (DFNB21, {603629})
Allelic disorder to autosomal recessive form ({224900})
Allelic disorder to autosomal recessive hearing loss (DFNB2
Allelic disorder to autosomal recessive inclusion body myopathy-2 (IBM2, {600737})
Allelic disorder to benign hereditary chorea ({118700}), which is less severe
Allelic disorder to benign recurrent intrahepatic cholestasis (BRIC, {243300})
Allelic disorder to benign recurrent intrahepatic cholestasis (BRIC1, {243300})
Allelic disorder to branchiootic syndrome (BOS1, {602588}) and otofaciocervical syndrome ({166780})
Allelic disorder to branchiootorenal syndrome (BOR, {113650}) and otofaciocervical syndrome ({166780})
Allelic disorder to Charcot-Marie-Tooth disease 2F (CMT2F, {606595})
Allelic disorder to Charcot-Marie-Tooth disease type 1A ({118220})
Allelic disorder to Charcot-Marie-Tooth disease type 2A2 (CMT2A2, {609260})
Allelic disorder to Charcot-Marie-Tooth disease type 2D (CMT2D, {601472}), but distinguished by less severe distal sensory involvement
Allelic disorder to choreoathetosis, congenital hypothyroidism, and neonatal respiratory distress ({610978}), which is a more severe disorder
Allelic disorder to CLN8 ({600143})
Allelic disorder to CMT4A ({214400})
Allelic disorder to congenital muscular dystrophy type 1C (MDC1C, {606612})
Allelic disorder to corticosterone methyloxidase type I deficiency ({203400})
Allelic disorder to corticosterone methyloxidase type II deficiency ({610600})
Allelic disorder to dilated cardiomyopathy 1N (CMD1N, {607487})
Allelic disorder to distal spinal muscular atrophy type V (DSMAV, {600794}), but distinguished by more severe distal sensory involvement
Allelic disorder to distal spinal muscular atrophy, type V (DSMAV, {600794}), but distinguished by the presence of spasticity
Allelic disorder to Dunnigan-type familial partial lipodystrophy ({151660})
Allelic disorder to EBS Dowling-Meara ({131760}), EBS Koebner ({131900}), and EBS Weber-Cockayne ({131800})
Allelic disorder to ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 (EEC3, {604292})
Allelic disorder to episodic ataxia 2 (EA2, {108500})
Allelic disorder to episodic ataxia-2 (EA2, {108500}) and spinocerebellar ataxia-6 (SCA6, {183086})
Allelic disorder to familial cylindromatosis ({132700}) and Brooke-Spielger syndrome (BSS, {605041})
Allelic disorder to familial hemiplegic migraine 1 (FHM1, {141500})
Allelic disorder to familial hypertrophic cardiomyopathy (CMH, {192600})
Allelic disorder to generalized epilepsy with seizures-plus (GEFS+, {604233})
Allelic disorder to hyperkalemic periodic paralysis (HYPP, {170500})
Allelic disorder to hyperkalemic periodic paralysis (HYPP, {608390})
Allelic disorder to hyperostosis-hyperphosphatemia syndrome ({610233})
Allelic disorder to hyperphosphatemic familial tumoral calcinosis (HFTC, {211900})
Allelic disorder to hypokalemic periodic paralysis (HOKPP, {170400})
Allelic disorder to infantile neuroaxonal dystrophy ({256600}
Allelic disorder to infantile-onset ascending spastic paralysis (IAHSP, {607225})
Allelic disorder to intrahepatic cholestasis of pregnancy (ICP, {147480})
Allelic disorder to juvenile amyotrophic lateral sclerosis 2 (ALS2, {205100})
Allelic disorder to juvenile nephronophthisis-1 ({256100})
Allelic disorder to juvenile primary lateral sclerosis (PLSJ, {606353})
Allelic disorder to juvenile-onset amyotrophic lateral sclerosis (ALS2, {205100})
Allelic disorder to Karak syndrome ({608395})
Allelic disorder to limb girdle muscular dystrophy type 1C (LGMD1C, {607801})
Allelic disorder to Limb-Girdle Muscular Dystrophy type 2B (LGMD2B, {253601})
Allelic disorder to limb-girdle muscular dystrophy type 2I (LGMD2I, {607155})
Allelic disorder to limb-mammary syndrome (LMS, {603543})
Allelic disorder to long QT syndrome-1 (LQT1, {192500})
Allelic disorder to Margarita Island type of ectodermal dysplasia ({225060})
Allelic disorder to Miyoshi myopathy ({254130}) and distal myopathy with anterior tibial onset ({606768})
Allelic disorder to multiple familial trichoepithelioma 1 (MFT1, {601606}) and Brooke-Spiegler syndrome (BSS, {605041})
Allelic disorder to multiple familial trichoepithelioma 1 (MFT1, {601606}) and familial cylindromatosis (FC, {132700})
Allelic disorder to NF1
Allelic disorder to Nieman-Pick disease type B ({607616})
Allelic disorder to Niemann-Pick disease type A ({257200})
Allelic disorder to Nonaka myopathy ({605820})
Allelic disorder to Northern epilepsy ({610003})
Allelic disorder to Opitz-Kaveggia syndrome ({305450})
Allelic disorder to orofaciodigital syndrome 1 (OFD1, {311200})
Allelic disorder to OSMED ({215150}) Allelic disorder to Weissenbacher-Zweymuller syndrome ({277610})
Allelic disorder to osteoporosis-pseudoglioma syndrome (OPPG, {259770})
Allelic disorder to paramyotonia congenita ({168300})
Allelic disorder to Parkinson disease-1 (PARK1, {168601})
Allelic disorder to PFIC3 ({602347})
Allelic disorder to potassium-aggravated myotonia ({608390})
Allelic disorder to primary erythermalgia ({133020})
Allelic disorder to primary microcephaly ({251200})
Allelic disorder to progressive familial intrahepatic cholestasis-1 (PFIC1, {211600})
Allelic disorder to progressive familial intrahepatic cholestasis-2 (PFIC2, {601847})
Allelic disorder to Rapp-Hodgkin syndrome (RHS, {129400})
Allelic disorder to Rett syndrome ({312750})
Allelic disorder to rigid spine muscular dystrophy (RSMD1, {602771})
Allelic disorder to rippling muscle disease (RMD, {606072})
Allelic disorder to Schindler disease ({609241})
Allelic disorder to Silver syndrome ({270685}), but distinguished by lack of spasticity
Allelic disorder to spinal muscular atrophy type I ({253300})
Allelic disorder to split-hand/foot malformation 4 (SHFM4, {605289})
Allelic disorder to Stickler syndrome 3 ({184840})
Allelic disorder to T cell-negative, B cell-negative, NK cell- negative SCID ({601457}), which is more severe
Allelic disorder to the IVIC syndrome ({147750})
Allelic disorder to the Zlotogora-Ogur syndrome ({225000})
Allelic disorder to type IV glycogen storage disease ({232500})
Allelic disorder to Usher syndrome type 1F ({602083})
Allelic disorder to van der Woude syndrome (VWS, {119300}) and popliteal pterygium syndrome (PPS, {119500})
Allelic disorder to Walker-Warburg syndrome ({236670})
Allelic disorders with clinical overlap include DSS and CMT1B ({118200})
Allelic disorders with overlapping phenotypes include autosomal dominant Emery-Dreifuss muscular dystrophy ({181350}) and dilated cardiomyopathy type 1A ({115200})
Allelic disorders with overlapping phenotypes include Charcot-Marie-Tooth disease type 1 (CMT1B, {118200} and CMT1A, {118220}) and Dejerine-Sottas syndrome (DSS, {145900})
Allelic disorders with overlapping phenotypes include CMT1A ({118220}), hereditary neuropathy with liability to pressure palsies (HNPP, {162500}), and Dejerine-Sottas syndrome (DSS, {145900})
Allelic disorders with overlapping phenotypes include congenital hypomyelinating neuropathy (CHN, {605253}) and Dejerine-Sottas syndrome (DSS, {145900})
Allelic disorders with overlapping phenotypes include Dejerine-Sottas syndrome (DSS, {145900}), hereditary neuropathy with liability to pressure palsies (HNPP, {162500}), and CMT with deafness ({118300})
Allelic disorders with overlapping phenotypes include DSS, congenital hypomyelination (CHN, {605253}), and some forms of axonal CMT2 (see {607677})
Allelic disorders with overlapping phenotypes include hereditary lymphedema type II ({153200}), lymphedema and ptosis ({153000}), and the lymphedema-distichiasis syndrome ({153400})
Allelic disorders with overlapping phenotypes include hereditary lymphedema type II ({153200}), lymphedema and ptosis ({153000}), and yellow nail and lymphedema syndrome ({153300})
Allelic disorders with overlapping phenotypes include the lymphedema-distichisis syndrome ({153400}), lymphedema and ptosis ({153000}), and yellow nail and lymphedema syndrome ({153300})
allelic frequency
allelic gene
Allelic Imbalance
Allelic Imbalances
Allelic Loss
Allelic loss on 16p13.3 in angiomyolipoma, cardiac rhabdomyoma, cortical tuber, and giant cell astrocytoma (TSC2)
Allelic Losses
Allelic state
Allelic state Bld/T
Allelic state in Blood or Tissue by Molecular genetics method
Allelic state:Find:Pt:Bld/Tiss:Nom:Molgen
Allelic state:Finding:Point in time:Whole blood/Tissue, unspecified:Nominal:MOLECULAR GENETICS
Allelic to acrocapitofemoral dysplasia ({607778})
Allelic to acrokeratosis verruciformis ({101900})
Allelic to acromesomelic dysplasia, Hunter-Thompson type ({201250}), brachydactyly, type C ({113100}), and fibular hypoplasia nd complex brachydactyly ({228900})
Allelic to ADULT syndrome ({103285}), SHFM4 ({605289}), Hay-Wells syndrome ({106260}), and limb-mammary syndrome ({603543})
Allelic to ADULT syndrome ({103285}), split hand/foot malformation 4 ({605289}), Rapp-Hodgkin syndrome ({129400}), Hay-Wells syndrome ({106260}), and limb-mammary syndrome ({603543})
Allelic to Aicardi-Goutieres syndrome ({225750})
Allelic to anterior segment mesenchymal dysgenesis ({107250})
Allelic to atelosteogenesis, type II ({256050}), achondrogenesis, type Ib ({600972}), and multiple epiphyseal dysplasia, type 4 ({226900})
Allelic to autosomal recessive PXE ({264800})
Allelic to Bannayan-Riley-Ruvalcaba syndrome ({153480}), which has an earlier age at onset
Allelic to Bardet-Biedel syndrome 6 ({209900})
Allelic to Birt-Hogg-Dube syndrome ({135150})
Allelic to brachydactyly type B ({113000})
Allelic to brachydactyly, type A1 ({112500})
Allelic to brachydactyly, type A2 ({112600})
Allelic to cartilage-hair hypoplasia ({250250})
Allelic to craniometaphyseal dysplasia ({123000})
Allelic to deafness, autosomal recessive 1, ({220290}), deafness, autosomal dominant 3, ({601544}), keratoderma, palmoplantar, with deafness, ({148350}), keratitis-ichthyosis-deafness syndrome, ({148210}), hystrix-like ichthyosis with deafness, ({602540})
Allelic to deafness, autosomal recessive 1, ({220290}), deafness, autosomal dominant 3, ({601544}), Vohwinkel syndrome, ({124500}), keratitis-ichthyosis-deafness syndrome, ({148210}), hystrix-like ichthyosis with deafness, ({602540}), Bart-Pumphrey syndro
Allelic to deafness, autosomal recessive 12 ({601386})
Allelic to deafness, autosomal recessive 23 ({609533})
Allelic to deafness, neurosensory, autosomal recessive 18 ({602092})
Allelic to dentin dysplasia, type 2 ({125420})
Allelic to dentinogenesis imperfecta 1 ({125490})
Allelic to diastrophic dysplasia ({222600}), achondrogenesis, type 1b ({600972}), and multiple epiphyseal dysplasia, type 4 ({226900})
Allelic to diastrophic dysplasia ({222600}), atelosteogenesis, type II ({256050}), and achondrogenesis, type IB ({600972})
Allelic to Dyggve-Melchior-Clausen disease ({223800})
Allelic to early-onset familial Alzheimer disease
Allelic to EEC3 ({604292}), SHFM4 ({605289}), ADULT syndrome ({103285}), limb-mammary syndrome ({603543}), and Rapp-Hodgkin syndrome ({129400})
Allelic to EEC3 ({604292}), SHFM4 ({605289}), Rapp-Hodgkin syndrome ({129400}), Hay-Wells syndrome ({106260}), and ADULT syndrome ({103285})
Allelic to Ellis-van Creveld syndrome ({225500})
Allelic to enhanced S-cone syndrome ({268100})
Allelic to Fechtner syndrome ({153640}), May-Hegglin anomaly ({155100}), Sebastian syndrome ({605249}), and Epstein syndrome ({153650})
Allelic to fibular aplasia or hypoplasia, femoral bowing, and poly-, syn-, and oligodactyly (Fuhrmann syndrome, {228930})
Allelic to fumarase deficiency ({606812}) and hereditary leiomyomatosis and renal cell cancer ({605839})
Allelic to Giant Platelet Syndrome ({231200}) and Bernard-Soulier Syndrome, benign, autosomal dominant ({153670})
Allelic to Grebe syndrome ({200700}), brachydactyly type C ({113100}), and acromesomelic dysplasia, Hunter-Thompson type ({201250})
Allelic to Grebe syndrome ({200700}), brachydactyly, type C ({113100}), fibular hypoplasia and complex brachydactyly ({228900})
Allelic to Grebe syndrome ({200700}), Du Pan syndrome ({228900}), and acromesomelic dysplasia, Hunter Thompson type ({201250})
Allelic to Groenouw type 1 corneal dystrophy ({121900}), Thiel-Behnke corneal dystrophy ({602082}), lattice type 1 corneal dystrophy ({122200}), lattice type IIIA corneal dystrophy ({608471}), and Reis-Bucklers type corneal dystrophy ({608470})
Allelic to hand osteoarthritis ({607850})
Allelic to HARP syndrome ({607236})
Allelic to Hawkinsinuria ({140350})
Allelic to hereditary multiple leiomyoma of skin ({150800}) and hereditary leiomyomatosis and renal cell cancer ({605839})
Allelic to Hoyeraal-Hreidarsson syndrome ({300240})
Allelic to hydropic and prenatally lethal chondrodystrophy ({215140})
Allelic to hyperimmunoglobulinemia D syndrome (HIDS, {260920})
Allelic to hypoparathyroidism-retardation-dysmorphism syndrome ({241410})
Allelic to infantile sialic acid storage disorder ({269920})
Allelic to infantile systemic hyalinosis ({236490})
Allelic to Joubert syndrome 5 ({610188}) and Leber congenital amaurosis type X ({610142})
Allelic to Kenny-Caffey syndrome type 2 ({244460})
Allelic to LEOPARD syndrome ({151100})
Allelic to leprechaunism ({246200}) and insulin-resistant diabetes mellitus with acanthosis nigricans ({147670})
Allelic to Marshall syndrome ({154780})
Allelic to May-Hegglin anomaly ({155100}), Fechtner syndrome ({153640}), Epstein syndrome ({153650}) and deafness, autosomal dominant 17 ({603622})
Allelic to May-Heglin anomaly ({155100}), Sebastian syndrome ({605249}), Epstein syndrome ({153650}), and deafness, autosomal dominant 17 ({603622})
Allelic to Meckel syndrome, type 3 ({607361})
Allelic to metaphyseal dysplasia without hypotrichosis ({250460})
Allelic to mevalonic aciduria ({610377})
Allelic to mucolipidosis II ({252500})
Allelic to mucopolysaccharidosis IVB
Allelic to multiple epiphyseal dysplasia, type 5 ({607078}) and hand osteoarthritis ({607850})
Allelic to multiple pterygium syndrome, lethal type ({253290})
Allelic to multiple synostoses syndrome 1 ({186500}), tarsal-carpal coalition syndrome ({186570}), and stapes ankylosis syndrome without symphalangism ({184460})
Allelic to Naxos disease ({601214})
Allelic to nephronophthisis 4 ({606966})
Allelic to neurofibromatosis-1 (NF1, {162200})
Allelic to Noonan syndrome ({163950})
Allelic to OSMED ({215150}) and Weissenbacher-Zweymuller syndrome ({277610})
Allelic to osteogenesis imperfecta type VII ({610682})
Allelic to osteopetrosis ({259700})
Allelic to osteoporosis-pseudoglioma syndrome ({259770}), van Buchem type 2 ({607636}), autosomal dominant osteosclerosis ({144750}), type I osteopetrosis ({607634})
Allelic to osteoporosis-pseudoglioma syndrome ({259770}), van Buchem type 2 ({607636}), high bone mass ({601884}), autosomal dominant endosteal hyperostosis ({144750})
Allelic to pachyonychia congenita Jackson-Lawler type ({167210})
Allelic to pantothenate kinase-associated neurodegeneration ({234200})
Allelic to Papillon-Lefevre syndrome ({245000}) and juvenile periodontitis ({170650})
Allelic to Pelger-Huet anomaly ({169400})
Allelic to premature chromosome condensation with microcephaly and mental retardation ({606858})
Allelic to proximal symphalangism ({185800}), multiple synostoses syndrome ({186500}), and stapes ankylosis syndrome without symphalangism ({184460})
Allelic to proximal symphalangism ({185800}), multiple synostoses syndrome ({186500}), and tarsal-carpal coalition syndrome ({186570})
Allelic to proximal symphalangism ({185800}), multiple synostoses syndrome 1 ({186500}), tarsal-carpal coalition syndrome ({186570}), and stapes ankylosis syndrome without symphalangism ({184460})
Allelic to proximal symphalangism ({185800}), stapes ankylosis syndrome without symphalangism ({184460}), and tarsal-carpal coalition syndrome ({186570})
Allelic to pseudoachondroplasia ({177170})
Allelic to retinitis punctata albescens ({136880}), fundus albipunctatus ({136880}), autosomal recessive retinitis pigmentosa ({268000}), Newfoundland rod-cone dystrophy ({607476})
Allelic to Rett syndrome ({312750})
Allelic to Roberts syndrome ({268300})
Allelic to Robinow syndrome, autosomal recessive ({268310})
Allelic to Senior-Loken syndrome 1 ({266900}) and Joubert syndrome 4 ({609583})
Allelic to Senior-Loken syndrome 4 ({606996})
Allelic to Senior-Loken syndrome 6 ({610189}) and Leber congenital amaurosis type X ({610142})
Allelic to several forms of autosomal recessive CMT (see {214400})
Allelic to Sialuria, Finnish type ({604369})
Allelic to spondyloepimetaphyseal dysplasia, MATN-3 related ({608728})
Allelic to Stickler syndrome, type 3 ({184840}) and OSMED ({215150})
Allelic to Stickler syndrome, type 3 ({184840}) and Weissenbacher-Zweymuller syndrome ({277610})
Allelic to thrombocytopenia, platelet dysfunction, hemolysis, and imbalanced globin synthesis ({314050})
Allelic to trichorhinophalangeal syndrome, type III (TRPS3, {190351})
Allelic to TRP1 ({190350})
Allelic to type I osteopetrosis ({607634}), osteoporosis-pseudoglioma ({259770}), high bone mass ({601884}), autosomal dominant endosteal hyperostosis ({144750})
Allelic to type I osteopetrosis ({607634}), osteoporosis-pseudoglioma ({259770}), type II van Buchem disease ({607636}), and high bone mass ({601884})
Allelic to tyrosinemia, type III ({276720})
Allelic to ulnar and fibula, absence of, with severe limb deficiency (Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome {276820})
Allelic to Usher syndrome, type ID ({601067})
Allelic to Vohwinkel syndrome, variant form ({604117})
Allelic to Waardenburg syndrome, type IIA ({193510})
Allelic to Wiskott-Aldrich syndrome ({301000}) and severe congenital X-linked neutropenia ({300299})
Allelic to Wiskott-Aldrich syndrome ({301000}) and X-linked thrombocytopenia ({313900})
Allelic to X-linked hydrocephalus ({307000}) and X-linked spastic paraplegia ({312900})
Allelic with cone-rod dystrophy 10 ({610283})
Allelic with Cowden disease ({158350})
Allelic with dentinogenesis imperfecta 1 ({125490}) and dentin dysplasia, type II ({125420})
Allelic with Papillon-Lefevre syndrome ({245000}) and Haim-Munk syndrome ({245010})
Allelic with Smith-McCort dysplasia ({607326})
Allelic with some cases of aplastic anemia ({609135})
Allelism Test
Allelism Tests
Allelochemicals
Allelomorph
Allelomorphs
allelopathies
Allelotype Analysis
Allelotype Profiling
Allelotyping
alleluia
allemandes
Allen
Allen & Hanburys Brand of Acetylcysteine
Allen & Hanburys Brand of Beclomethasone Dipropionate
Allen & Hanburys Brand of Dequalinium Chloride
Allen Canyon
Allen Canyon Indians
Allen Intestinal Forceps
Allen key
Allen picture test
Allen screw
Allen screws
Allen test
allen wrench
allen wrenches
Allen's Gallinule (Porphyrio alleni)
Allen's Hummingbird
Allenanthus
Allenanthus hondurensis
Allenbatrachus
Allenbatrachus grunniens
allene
allene oxide cyclase
allene oxide cyclase 2, Arabidopsis
allene oxide synthase
allene oxide synthase activity
Allene oxide synthase-lipoxygenase protein, Plexaura homomalla
Allene oxide synthase, Parthenium argentatum
Allene-oxide cyclase
allene-oxide cyclase activity
allenes
Allenhyphes
Allenhyphes flinti
Allenia fusca
allenolic acid
Allenopithecus
Allenopithecus nigroviridis
Allenrolfea
Allenrolfea occidentalis
Allenrolfea occidentalis Ab.IgE
Allenrolfea occidentalis Ab.IgE:ACnc:Pt:Ser:Qn
Allenrolfea occidentalis Ab.IgE.RAST class
Allenrolfea occidentalis Ab.IgE.RAST class:ACnc:Pt:Ser:Ord
Allenrolfea occidentalis Antibody.immunoglobulin E
Allenrolfea occidentalis Antibody.immunoglobulin E:Arbitrary Concentration:Point in time:Serum:Quantitative
Allenrolfea occidentalis Antibody.immunoglobulin E.RAST class
Allenrolfea occidentalis Antibody.immunoglobulin E.RAST class:Arbitrary Concentration:Point in time:Serum:Ordinal
Allenrolfea occidentalis antigen
ALLENROLFEA OCCIDENTALIS POLLEN
ALLENROLFEA OCCIDENTALIS POLLEN 0.05 g in 1 mL INTRADERMAL INJECTION, SOLUTION
ALLENROLFEA OCCIDENTALIS POLLEN 0.05 g in 1 mL SUBCUTANEOUS INJECTION, SOLUTION
ALLENROLFEA OCCIDENTALIS POLLEN 0.1 g in 1 mL INTRADERMAL INJECTION, SOLUTION
ALLENROLFEA OCCIDENTALIS POLLEN 0.1 g in 1 mL SUBCUTANEOUS INJECTION, SOLUTION
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