AI & ChatGPT searches , social queriess for PAGON
Search references for PAGON. Phrases containing PAGON
See searches and references containing PAGON!
Search references for PAGON. Phrases containing PAGON
See searches and references containing PAGON!PAGON
Comics character
Pagon is a character appearing in American comic books published by Marvel Comics. Created by writer Brian Michael Bendis and artist David Finch, the
Pagon
Hill in Temburong District, Brunei
Bukit Pagon (BOO-kit PAH-gon) is the highest point in the country, rising to an elevation of 1,841 metres (6,040 ft) above sea level. It is located in
Bukit_Pagon
Jamaican cricketer (born 1982)
Donovan Jomo Pagon (born 13 September 1982) is a West Indian cricketer. He attended Wolmer's Schools. He has the record for the highest ever individual
Donovan_Pagon
Jamaican tennis player (born 1988)
Dominic Pagon (born March 8, 1988) is a Jamaican professional tennis player. Pagon has an International Tennis Federation win–loss record of 21–28 primarily
Dominic_Pagon
American film producer
Blye Pagon Faust is an American film, television, and audio producer for the production company Story Force Entertainment. Blye Pagon Faust was raised
Blye_Pagon_Faust
Ancient Egyptian religion was a complex system of polytheistic beliefs and rituals that formed an integral part of ancient Egyptian culture. It centered
Ancient_Egyptian_religion
Village on the island of Corfu, Greece
Pagoi had 131 inhabitants at the 2021 census. The village Agios Georgios Pagon had 62 inhabitants at the 2021 census. It was developed as a tourist resort
Pagoi
Medical condition
syndrome, HARD syndrome (Hydrocephalus, Agyria and Retinal Dysplasia), Pagon syndrome, cerebroocular dysgenesis (COD) or cerebroocular dysplasia-muscular
Walker–Warburg_syndrome
Genetic disorder
List of syndromes Characteristics of syndromic ASD conditions Morris, CA; Pagon, RA; Adam, MP; Ardinger, HH; Wallace, SE; Amemiya, A; Bean, LJH; Bird, TD;
Williams_syndrome
2023 Marvel Studios television miniseries
as a child. Killian Scott as Pagon: A rebel Skrull and Gravik's second-in-command. Ben-Adir said Gravik sees that Pagon has ambition and wants to be a
Secret_Invasion_(miniseries)
Medical condition
SIDEROBLASTIC, AND SPINOCEREBELLAR ATAXIA; ASAT". omim.org. Retrieved 2022-06-11. Pagon, R. A.; Bird, T. D.; Detter, J. C.; Pierce, I. (1985-08-01). "Hereditary
X-linked sideroblastic anemia and spinocerebellar ataxia
X-linked_sideroblastic_anemia_and_spinocerebellar_ataxia
Irish actor
2019 Dublin Murders Detective Rob Reilly Main role 2023 Secret Invasion Pagon Miniseries, main role 2024 Kaos Orpheus Main role 2026 The Capture Commander
Killian_Scott
Genetic condition involving facial, heart, blood and skeletal features
Judith E.; Roberts, Amy E. (1993), Adam, Margaret P.; Ardinger, Holly H.; Pagon, Roberta A.; Wallace, Stephanie E. (eds.), "Noonan Syndrome", GeneReviews®
Noonan_syndrome
2021 American documentary miniseries
Jenner Furst and Julia Willoughby Nason and executive produced by Blye Pagon Faust and Cori Shepherd Stern. It follows LuLaRoe, a clothing empire accused
LuLaRich
Medical condition
Indo, Yasuhiro (1993), Adam, Margaret P.; Bick, Sarah; Mirzaa, Ghayda M.; Pagon, Roberta A. (eds.), "NTRK1 Congenital Insensitivity to Pain with Anhidrosis"
Congenital insensitivity to pain with anhidrosis
Congenital_insensitivity_to_pain_with_anhidrosis
Medical condition
microcephaly". Orphanet. Biesecker, L. G.; Adam, M. P.; Ardinger, H. H.; Pagon, R. A.; Wallace, S. E.; Bean LJH; Gripp, K. W.; Mirzaa, G. M.; Amemiya,
Amish_lethal_microcephaly
Metabolic disorders in which porphyrins build up in the body
PMID 28630774. Wang, B.; Bissell, D. M.; Adam, M. P.; Ardinger, H. H.; Pagon, R. A.; Wallace, S. E.; Bean LJH; Stephens, K.; Amemiya, A. (2018). "Hereditary
Porphyria
Three genetic disorders involving benign tumors of the nervous system
Plotkin S, Asthagiri A, Messiaen L, Babovic-Vuksanovic D, Adam MP, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A (1993). "LZTR1- and SMARCB1-Related
Neurofibromatosis
Genetic condition, the most common form of dwarfism
PMID 17630040. S2CID 208788746. Pauli RM, Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean L, Mefford HC, Stephens K, Amemiya A, Ledbetter N (2012)
Achondroplasia
Collection of signs that resemble Marfan syndrome
(1): 293–301. doi:10.1245/s10434-007-9665-4. PMID 17963006. S2CID 2564555. Pagon, RA.; Bird, TC.; Dolan, CR.; Stephens, K.; Picker, JD.; Levy, HL. (1993)
Marfanoid
2023 American TV series or program
Willoughby Nason, and also executive produced by Cori Shepherd Stern, Blye Pagon Faust, Mike Gasparro, Jody McVeigh-Schultz, and Jenner Furst. Jill Duggar
Shiny Happy People (TV series)
Shiny_Happy_People_(TV_series)
Medical condition
Kagami, Masayo (1993), Adam, Margaret P.; Feldman, Jerry; Mirzaa, Ghayda M.; Pagon, Roberta A. (eds.), "Kagami-Ogata Syndrome", GeneReviews®, Seattle (WA):
Kagami–Ogata_syndrome
Medical condition
Reichenberger, Ernst; Chen, I.-Ping (1993), Adam, Margaret P.; Ardinger, Holly H.; Pagon, Roberta A.; Wallace, Stephanie E. (eds.), "Craniometaphyseal Dysplasia
Craniodiaphyseal_dysplasia
Medical condition
Steeves M, Parkin K, Thibert R (1993), Adam MP, Feldman J, Mirzaa GM, Pagon RA (eds.), "Pitt-Hopkins Syndrome", GeneReviews®, Seattle (WA): University
Pitt–Hopkins_syndrome
Abnormal development, at macroscopic or microscopical level
"Fibrous Dysplasia/McCune–Albright Syndrome". In Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJ, Mirzaa G, Amemiya A (eds.). Gene Reviews. Seattle
Dysplasia
Progressive neurological disease
Lateral Sclerosis and Frontotemporal Dementia". In Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJ, Stephens K, Amemiya A (eds.). GeneReviews. University
Spinocerebellar_ataxia
Rare medical conditions that result in easy blistering of the skin and mucous membranes
ISBN 0-07-138076-0. So JY, Teng J (1993), Adam MP, Bick S, Mirzaa GM, Pagon RA (eds.), "Epidermolysis Bullosa Simplex", GeneReviews®, Seattle (WA):
Epidermolysis_bullosa
Aruba 1 1 2 3 1 Dominic Pagon Clifford Giel 6 3 2 6 4 6 2 Damion Johnson Gian Hodgson 6 4 6 4 3 Damion Johnson / Dominic Pagon Clifford Giel / Gian
2010 Davis Cup Americas Zone Group III
2010_Davis_Cup_Americas_Zone_Group_III
2008 Marvel Comics event
the leader of the ninja group the Hand, is revealed to be a Skrull named Pagon after dying in battle with the New Avengers. Veranke takes the corpse to
Secret_Invasion
Medical condition
PMID 10464653. Smith RJ (1993-01-01). "Branchiootorenal Spectrum Disorder". In Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJ, et al. (eds.)
Branchio-oto-renal_syndrome
Skin which is abnormally inelastic and hangs loosely
NBK5201. In Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A (1993). Pagon RA, Bird TD, Dolan CR, et al. (eds.). GeneReviews
Cutis_laxa
243 ft) Philippines * Mount Mandalagan 1,885 m (6,184 ft) Philippines * Bukit Pagon 1,850 m (6,070 ft) Brunei * Khao Luang 1,840 m (6,037 ft) Thailand * Phnom
List of Southeast Asian mountains
List_of_Southeast_Asian_mountains
Autosomal recessive metabolic disorder
Farnham KM, Atwal HK, Macklin S, et al. (2020). Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJ, Gripp KW, Mirzaa GM, Amemiya A (eds.). "Maple Syrup
Maple_syrup_urine_disease
Medical condition
Contractural Arachnodactyly". In Adam, Margaret P.; Ardinger, Holly H.; Pagon, Roberta A.; Wallace, Stephanie E.; Bean, Lora JH; Stephens, Karen; Amemiya
Congenital contractural arachnodactyly
Congenital_contractural_arachnodactyly
Genus of moths
Lymantria ornata Oberthür, 1923 Lymantria ossea Toxopeus, 1948 Lymantria pagon Holloway, 1999 Lymantria panthera van Eecke, 1928 Lymantria pelospila Turner
Lymantria
Medical condition
Joyce (1993), Adam, Margaret P.; Everman, David B.; Mirzaa, Ghayda M.; Pagon, Roberta A. (eds.), "Epidermolysis Bullosa Simplex", GeneReviews®, Seattle
Epidermolysis_bullosa_simplex
Cricinfo. ESPN. Retrieved 2010-06-29. "Players / West Indies / Donovan Pagon". Cricinfo. ESPN. Retrieved 2010-06-29. "Players / West Indies / Dwight
List of international cricketers from Jamaica
List_of_international_cricketers_from_Jamaica
Rare autosomal dominant cancer syndrome
Ortrud K. (1993), Adam, Margaret P.; Feldman, Jerry; Mirzaa, Ghayda M.; Pagon, Roberta A. (eds.), "Birt-Hogg-Dubé Syndrome", GeneReviews®, Seattle (WA):
Birt–Hogg–Dubé_syndrome
Mitochondrial disorder
Hirano, Michio (1993). "MERRF". In Adam, Margaret P.; Ardinger, Holly H.; Pagon, Roberta A.; Wallace, Stephanie E.; Bean, Lora J.H.; Mefford, Heather C
MERRF_syndrome
Ridge on the cerebral cortex of the brain
23 (1): 225–41. PMID 3472611. Chang, B; Walsh, CA; Apse, K; Bodell, A; Pagon, RA; Adam, TD; Bird, CR; Dolan, K; Fong, MP; Stephens, K (1993). "Polymicrogyria
Gyrus
Medical condition for inability to feel pain
Geoffrey (1993), Adam, Margaret P.; Feldman, Jerry; Mirzaa, Ghayda M.; Pagon, Roberta A. (eds.), "Congenital Insensitivity to Pain Overview", GeneReviews®
Congenital insensitivity to pain
Congenital_insensitivity_to_pain
Species of moth
vicarians Amata vicarians api Holloway, 1988 (Sarawak) Amata vicarians pagon (Holloway, 1988) (Brunei) "Amata (Genus)". ZipcodeZoo.com. Archived from
Amata_vicarians
Congenital condition where an individual with a 46,XX karyotype is male
"Nonsyndromic 46,XX Testicular Disorders/Differences of Sex Development". In Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean L, Bird TD, Fong CT
XX_male_syndrome
Amino acid
Charles P. (1993), Adam, Margaret P.; Feldman, Jerry; Mirzaa, Ghayda M.; Pagon, Roberta A. (eds.), "Isolated Methylmalonic Acidemia", GeneReviews®, Seattle
Threonine
2015 film directed by Tom McCarthy
Directed by Tom McCarthy Written by Josh Singer Tom McCarthy Produced by Blye Pagon Faust Steve Golin Nicole Rocklin Michael Sugar Starring Mark Ruffalo Michael
Spotlight_(film)
Medical condition
Steinberg SJ, Raymond GV, Braverman NE, et al. (2020). Adam MP, Ardinger HH, Pagon RA, et al. (eds.). "Zellweger Spectrum Disorder". GeneReviews® [Internet]
Peroxisomal_disorder
Medical condition
PMID 20301595. NBK1422. In Adam MP, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A (1993). Pagon RA, Bird TD, Dolan CR, et al. (eds.). GeneReviews
Nonsyndromic_deafness
Medical condition
Valentin, Ilia (1993), Adam, Margaret P.; Bick, Sarah; Mirzaa, Ghayda M.; Pagon, Roberta A. (eds.), "NR2F1-Related Neurodevelopmental Disorder", GeneReviews®
Bosch–Boonstra–Schaaf optic atrophy syndrome
Bosch–Boonstra–Schaaf_optic_atrophy_syndrome
Medical condition
University Press. p. 986. ISBN 0-19-511861-8. Stevenson, Roger E. (1993-01-01). Pagon, Roberta A.; Adam, Margaret P.; Ardinger, Holly H.; Wallace, Stephanie E
ATR-X_syndrome
Medical condition
NBK1500. In Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A (1993). Pagon RA, Bird TD, Dolan CR, et al. (eds.). GeneReviews
CADASIL
Medical condition
Lateral Meningocele Syndrome". In Adam, Margaret P.; Ardinger, Holly H.; Pagon, Roberta A.; Wallace, Stephanie E. (eds.). Lateral Meningocele Syndrome
Lateral_meningocele_syndrome
Chemical compound
Nesterova G, Gahl WA (6 October 2016). "Cystinosis". In Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJ, Stephens K, Amemiya A (eds.). GeneReviews. Seattle
Cysteamine
Cancerous tumor of the developing eye
Gallie BL (1993). "Retinoblastoma". In Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJ, Gripp KW, Amemiya A (eds.). GeneReviews®. Seattle
Retinoblastoma
American film awards
Xavier Dolan, Nancy Grant Canada 2016 (22nd) Spotlight Tom McCarthy Blye Pagon Faust, Steve Golin, Nicole Rocklin, Michael Sugar United States The Assassin
Chlotrudis Award for Best Movie
Chlotrudis_Award_for_Best_Movie
Academic database
heritable diseases. It was established in 1997 as GeneClinics by Roberta A Pagon (University of Washington) with funding from the National Institutes of
GeneReviews
Manama Bangladesh: Dinajpur, Rangpur City, Saidpur Bhutan: Thimphu1 Brunei: Pagon Hill1 Cambodia: Cardamom Mountains China: Beiliu, Changsha, Chengdu, Chongqing
List of locations with a subtropical climate
List_of_locations_with_a_subtropical_climate
Rare genetic disorder of the white matter of the brain
25, 1993). "Alexander Disease". In Adam, Margaret P.; Mirzaa, Ghayda M.; Pagon, Roberta A.; Wallace, Stephanie E.; Bean, Lora JH; Gripp, Karen W.; Amemiya
Alexander_disease
Rare genetic disease
2016. Lyons, Michael J. (1993), Adam, Margaret P.; Ardinger, Holly H.; Pagon, Roberta A.; Wallace, Stephanie E. (eds.), "MED12-Related Disorders", GeneReviews
FG_syndrome
Medical condition
PMID 4154122. Berry, Gerard T. (1993), Adam, Margaret P.; Mirzaa, Ghayda M.; Pagon, Roberta A.; Wallace, Stephanie E. (eds.), "Classic Galactosemia and Clinical
Galactosemia
Medical condition
Staudt, Martin (1993), Adam, Margaret P.; Feldman, Jerry; Mirzaa, Ghayda M.; Pagon, Roberta A. (eds.), "FOXG1 Syndrome", GeneReviews®, Seattle (WA): University
FOXG1_syndrome
Protein-coding gene in the species Homo sapiens
PMID 20301483. NBK1306. In Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE (2002). Pagon RA, Bird TD, Dolan CR, et al. (eds.). GeneReviews [Internet]
Sulfate_transporter
Medical condition
Marsha L; Wei, Chongjuan (July 25, 2013). "Peutz-Jeghers Syndrome". In Pagon, Roberta A; Adam, Margaret P; Bird, Thomas D; Dolan, Cynthia R; Fong, Chin-To;
Peutz–Jeghers_syndrome
Medical condition
Melissa P.; Caggana, Michele (1993), Adam, Margaret P.; Ardinger, Holly H.; Pagon, Roberta A.; Wallace, Stephanie E. (eds.), "Krabbe Disease", GeneReviews®
Krabbe_disease
Medical condition
atresia and some of the other related characteristic malformations, R. A. Pagon first coined the acronym CHARGE in 1981 to emphasize that this cluster of
CHARGE_syndrome
Medical condition
Hirano, Michio (May 3, 2011). "Mitochondrial DNA Deletion Syndromes". In Pagon, Roberta A; Adam, Margaret P; Ardinger, Holly H; Wallace, Stephanie E; Amemiya
Pearson_syndrome
Medical condition
Motor and Sensory Neuropathy with Agenesis of the Corpus Callosum". In Pagon, Roberta A.; Adam, Margaret P.; Ardinger, Holly H.; Wallace, Stephanie E
Andermann_syndrome
Hearing loss present at birth
Richard JH (1993), Adam, Margaret P.; Feldman, Jerry; Mirzaa, Ghayda M.; Pagon, Roberta A. (eds.), "Genetic Hearing Loss Overview", GeneReviews®, Seattle
Congenital_hearing_loss
Film award
Sachs, Jayne Baron Sherman, Jay Van Hoy 2015 Spotlight Tom McCarthy Blye Pagon Faust, Steve Golin, Nicole Rocklin, Michael Sugar Brooklyn John Crowley
AARP Movies for Grownups Award for Best Movie for Grownups
AARP_Movies_for_Grownups_Award_for_Best_Movie_for_Grownups
Group of genetic connective tissues disorders
(July 2018). "Classic Ehlers–Danlos Syndrome". In Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJ, Stephens K, Amemiya A (eds.). GeneReviews. University
Ehlers–Danlos_syndrome
Medical condition
2012-09-25. Retrieved 2015-07-30. Adam, M. P.; Feldman, J.; Mirzaa, G. M.; Pagon, R. A.; Wallace, S. E.; Bean LJH; Gripp, K. W.; Amemiya, A.; Chandra, S
X-linked_thrombocytopenia
Group of neurodegenerative disorders with associated iron accumulation in the brain
PMID 34909266. Gregory A, Hayflick S (28 February 2013). Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJ, Stephens K, Amemiya A (eds.). Neurodegeneration
Neurodegeneration with brain iron accumulation
Neurodegeneration_with_brain_iron_accumulation
Annual award by the Academy of Motion Picture Arts and Sciences
Jason Blum, Helen Estabrook, and David Lancaster 2015 (88th) Spotlight Blye Pagon Faust, Steve Golin, Nicole Rocklin, and Michael Sugar The Big Short Dede
Academy Award for Best Picture
Academy_Award_for_Best_Picture
Medical condition
management for physiotherapists. Butterworth Heinemann. ISBN 978-0-7506-5390-9. Pagon, RA.; Bird, TC.; Dolan, CR.; Stephens, K.; Picker, JD.; Levy, HL. (1993)
Arachnodactyly
Protein-coding gene in humans
PMID 17179987. Allanson JE, Roberts AE (8 August 2019). "Noonan Syndrome". In Pagon RA, Bird TD, Dolan CR, et al. (eds.). GeneReviews [Internet]. Seattle WA:
BRAF_(gene)
Medical condition
Francesca; Bentivegna, Angela (1993), Adam, Margaret P.; Ardinger, Holly H.; Pagon, Roberta A.; Wallace, Stephanie E. (eds.), "Juvenile Hemochromatosis", GeneReviews®
Juvenile_hemochromatosis
Medical condition
PMID 28630774. Wang, B.; Bissell, D. M.; Adam, M. P.; Ardinger, H. H.; Pagon, R. A.; Wallace, S. E.; Bean LJH; Stephens, K.; Amemiya, A. (2018). "Hereditary
Aminolevulinic acid dehydratase deficiency porphyria
Aminolevulinic_acid_dehydratase_deficiency_porphyria
Genetic disorder involving connective tissue
PMC 8775541. PMID 35055593. Greally MT (2010). "Shprintzen-Goldberg". In Pagon RA, Bird TD, Dolan CR, et al. (eds.). GeneReviews™ [Internet] (1993–). Seattle
Marfan_syndrome
Medical condition
2019-03-13. Stumpel C, Vos YJ (2015). "L1 Syndrome". In Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJ, Stephens K, Amemiya A (eds.). GeneReviews. University
L1_syndrome
Medical condition
SE, Krasnewich DM (1993). "PMM2-CDG (CDG-Ia)". In Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJ, Stephens K, Amemiya A (eds.). GeneReviews®. Seattle
PMM2_deficiency
Microcephaly combined with lissencephaly
Syndrome Spectrum Disorders". In Adam, Margaret P.; Ardinger, Holly H.; Pagon, Roberta A.; Wallace, Stephanie E.; Bean, Lora J.H.; Mefford, Heather C
Microlissencephaly
Intentional blackouts for protest
November 2011 there is also a campaign named A-pagón: No pagues centrales nucleares y de carbón (A-pagón: Don't pay for nuclear and coal-fired power stations)
Apagón
Protein-coding gene in the species Homo sapiens
Intracellular Cobalamin Metabolism". In Adam MP, Feldman J, Mirzaa GM, Pagon RA (eds.). GeneReviews®. Seattle (WA): University of Washington, Seattle
MMACHC
Medical condition
Schuelke, Markus (1993-01-01). "Ataxia with Vitamin e Deficiency". In Pagon, Roberta A.; Adam, Margaret P.; Ardinger, Holly H.; Wallace, Stephanie E
Familial isolated vitamin E deficiency
Familial_isolated_vitamin_E_deficiency
Genetic disorder of the skull and face
(11): 2914–25. doi:10.1093/hmg/ddu004. PMID 24419316. Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LH, Stephens K, Amemiya A, Robin NH, Falk MJ, Haldeman-Englert
Crouzon_syndrome
Group of metabolic disorders
PMID 6434839. {{cite book}}: |journal= ignored (help) Seashore, MR; Pagon, RA; Adam, MP; Ardinger, HH; Bird, TD; Dolan, CR; Fong, CT; Smith, RJH;
Organic_acidemia
Biochemistry. 9 9. doi:10.1186/1471-2091-9-9. PMC 2323002. PMID 18384687. Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, et al. (1993)
Hemojuvelin
Medical condition
Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, Adam MP, Hudgins L, Hannibal M (16 May 2013). Adam MP, Ardinger HH, Pagon RA, Wallace
Kabuki_syndrome
Type of collagen protein
Disorders. University of Washington, Seattle. NBK1503. In Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJ, Stephens K, et al., eds. (1993–2018). GeneReviews
Collagen_VI
Genetic disorder causing an exaggerated startle response
Tijssen MA, Rees MI (1993). "Hyperekplexia". In Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJ, Stephens K, Amemiya A (eds.). GeneReviews®. Seattle
Hyperekplexia
Type of localized bleeding in tissues outside blood vessels
Ehlers-Danlos Syndrome. 1999 Sep 2 [Updated 2019 Feb 21]. In: Adam MP, Ardinger HH, Pagon RA, et al., editors. GeneReviews® [Internet]. Seattle (WA): University of
Bruise
Medical condition
J. (1993). "HEXA Disorders". In Adam, Margaret P.; Ardinger, Holly H.; Pagon, Roberta A.; Wallace, Stephanie E. (eds.). Hexosaminidase A Deficiency.
GM2_gangliosidoses
Medical condition
Clifford E. (1993), Adam, Margaret P.; Feldman, Jerry; Mirzaa, Ghayda M.; Pagon, Roberta A. (eds.), "Alport Syndrome", GeneReviews®, Seattle (WA): University
Alport_syndrome
Metabolic disorder
Charles (1993), Adam, Margaret P.; Everman, David B.; Mirzaa, Ghayda M.; Pagon, Roberta A. (eds.), "Propionic Acidemia", GeneReviews®, Seattle (WA): University
Propionic_acidemia
Form of limb-girdle muscular dystrophy
increased levels of calpain-3. Angelini, C; Fanin, M; Adam, MP; Ardinger, HH; Pagon, RA; Wallace, SE; Bean, LJH; Stephens, K; Amemiya, A (1993). Calpainopathy
Calpainopathy
Medical condition
Fete, Mary (1993), Adam, Margaret P.; Feldman, Jerry; Mirzaa, Ghayda M.; Pagon, Roberta A. (eds.), "Hypohidrotic Ectodermal Dysplasia", GeneReviews®, Seattle
Hypohidrotic ectodermal dysplasia
Hypohidrotic_ectodermal_dysplasia
Autosomal recessive genetic disorder
Parisi, Melissa; Glass, Ian (1993), Adam, Margaret P.; Ardinger, Holly H.; Pagon, Roberta A.; Wallace, Stephanie E. (eds.), "Joubert Syndrome", GeneReviews®
Joubert_syndrome
Cancerous tumor of the pineal gland
(1993). "DICER1 Tumor Predisposition". In Adam MP, Everman DB, Mirzaa GM, Pagon RA (eds.). GeneReviews®. Seattle (WA): University of Washington, Seattle
Pineoblastoma
Mitochondrial gene coding for a protein involved in the respiratory chain
Wiley. pp. 581–620. ISBN 978-0-470-54784-7. Adam MP, Bick S, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, et al. (1993). "Melas". GeneReviews. PMID 20301411
MT-ND5
Subclass of glycerophospholipids
Braverman NE, Steinberg SJ, Fallatah W, et al. (2020). Adam MP, Ardinger HH, Pagon RA, et al. (eds.). "Rhizomelic Chondrodysplasia Punctata Type 1". GeneReviews®
Plasmalogen
Inherited neurodegenerative disorder
PMID 25432725. Caron NS, Wright GE, Hayden MR (2020). Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJ, Stephens K, Amemiya A (eds.). "Huntington Disease"
Huntington's_disease
PAGON
PAGON
PAGON
PAGON
Boy/Male
Indian, Punjabi, Sikh
Heart of God
Girl/Female
Bengali, Hindu, Indian, Kannada, Marathi, Sanskrit, Sindhi, Telugu
A River
Boy/Male
Hindu, Indian, Marathi
Star
Boy/Male
Hindu, Indian, Marathi, Tamil
The Sun
Girl/Female
Hindu, Indian, Telugu
Judicial
Surname or Lastname
English
English : habitational name from Kinton in Herefordshire, Kineton in Warwickshire (both named with Old English cyne- ‘royal’ + tūn ‘settlement’), or Kineton in Gloucestershire, which is named with Old English cyning ‘king’ + tūn.
Girl/Female
Muslim
Beautiful, Stubborn, Young princess
Boy/Male
Latin
Stutters.
Girl/Female
Hindu, Indian, Spanish
Graceful; Beautiful One
Girl/Female
Christian & English(British/American/Australian)
Fairy
PAGON
PAGON
PAGON
PAGON
PAGON