reduced results from

18 B

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options split into images, definition, symptoms, related diagnoses, diagnostic tests, therapies, and medications

category genetic or congenital, hand problems frequency rare (U.S.)

likelihood by age

likelyhood by duration of symptoms

related physician types genetics specialist family practitioner internist postal code Find Local The results are computer generated suggestions to help you find a physician. MEDgle does not recommend any particular type of physician or claim to be complete or accurate in the providers and specialties suggested.

familial brachydactyly - short fingers Definition for familial brachydactyly http://jmg.bmj.com/cgi/content/abstract/32/11/851 some common symptoms deformity of finger(s) permanent deflection of finger(s) short fingers and or toes some related diagnoses 1 - 7 of 28 diagnoses Down's Syndrome nail patella syndrome Holt-Oram Syndrome Prader-Willi Syndrome Turner's Syndrome Poland's Syndrome oralfacialdigital syndrome   more do i have 'familial brachydactyly'? In addition the following diagnostic tests might be need to help verify the diagnosis: diagnostic test search results for 'familial brachydactyly' 1 - 4 of 4 diagnostic tests X-ray foot (feet) familial brachydactyly and X-ray foot (feet) X-ray hand(s) familial brachydactyly and X-ray hand(s) Molecular Genetic Studies familial brachydactyly and Molecular Genetic Studies X-rays familial brachydactyly and X-rays therapeutic procedures for 'familial brachydactyly'? Managing or treating a diseases should always be determined by a patients health care provider. Below is a list of associated therapeutic procedures or medications for familial brachydactyly: therapeutic procedure search results for 'familial brachydactyly' 1 - 2 of 2 therapeutic procedures rankings are computer generated. please consult your health care provider. surgical intervention familial brachydactyly and surgical intervention X-ray foot (feet) familial brachydactyly and X-ray foot (feet) medications search results for 'familial brachydactyly' rankings are computer generated. please consult your health care provider. web search results for familial brachydactyly Web (All)  |  Treatment  |  Drugs  |  Tests  |  Research  |  Diet Results 1 - 50 - familial brachydactyly OMIM Update List for December, 1996 600771 FAMILIAL DWARFISM WITH MUSCLE SPASMS. 600858 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, WITH WOLFF-PARKINSON-WHITE ... 113200 BRACHYDACTYLY, TYPE D; BDD ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?12.1996   www.ncbi.nlm.nih.gov - summary OMIM Update List for December, 2002 Clinical Synopsis for 606835 DIGITAL ARTHROPATHY-BRACHYDACTYLY, FAMILIAL ... 606835 DIGITAL ARTHROPATHY-BRACHYDACTYLY, FAMILIAL. 607280 CONTACTIN 4; CNTN4 ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?12.2002   www.ncbi.nlm.nih.gov - summary OMIM Update List for March, 2004 605635 HYPERALDOSTERONISM, FAMILIAL, TYPE II ... 605982 FAMILIAL WILMS TUMOR 2 ... 607004 BRACHYDACTYLY, TYPE A1, B ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?3.2004   www.ncbi.nlm.nih.gov - summary SHORT STATURE - Pedbase.org 1. Familial Short Stature. 2. Constitutional Short Stature (Delayed Puberty) ... Brachydactyly E. Kallman's Syndrome. Klippel-Feil Anomaly. Leri-Weill Syndrome ... http://www.pedbase.org/s/short-stature   www.pedbase.org - summary OMIM Update List for July, 1996 Clinical Synopsis for 104110 ALOPECIA, FAMILIAL FOCAL ... Clinical Synopsis for 112450 BRACHYDACTYLY, PREAXIAL, WITH HALLUX VARUS AND THUMB ABDUCTION ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?7.1996   www.ncbi.nlm.nih.gov - summary OMIM Update List for July, 1997 112910 BRACHYDACTYLY, TYPE A6; BDA6. 120435 COLON CANCER, FAMILIAL, NONPOLYPOSIS TYPE 1; FCC1 ... RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 1; ARVD1 ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?7.1997   www.ncbi.nlm.nih.gov - summary Orphanet: Digital arthropathy brachydactyly, familial The portal for rare diseases and orphan drugs ... Digital arthropathy-brachydactyly, familial. Orpha number. ORPHA85169. Prevalence of rare diseases ... http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=85169   www.orpha.net - summary OMIM Update List for January, 2004 112500 BRACHYDACTYLY, TYPE A1; BDA1 ... 606835 DIGITAL ARTHROPATHY-BRACHYDACTYLY, FAMILIAL. 607060 PARKINSON DISEASE 8; PARK8 ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?1.2004   www.ncbi.nlm.nih.gov - summary OMIM Update List for January, 2008 142680 PERIODIC FEVER, FAMILIAL, AUTOSOMAL DOMINANT ... 611717 SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE SPEECH ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?1.2008   www.ncbi.nlm.nih.gov - summary APERT SYNDROME - Pedbase.org familial - autosomal dominant (de novo mutations in most cases) chrom.#: ? gene: ? M = F ? ... brachydactyly. continuous nailbeds. 2. Joints ... http://pedbase.org/a/apert-syndrome/   pedbase.org - summary OMIM Update List for February, 2009 603670 BLUE NEVI, FAMILIAL MULTIPLE ... CONVULSIONS, BENIGN FAMILIAL INFANTILE, 2; ... Clinical Synopsis for 228900 FIBULAR HYPOPLASIA AND COMPLEX BRACHYDACTYLY ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?2.2009   www.ncbi.nlm.nih.gov - summary Familial syndrome of progressive arterial occlusive disease consistent ... ... brachydactyly and syndactyly of the hands and feet, and increased bone fragility ... Explanations for this familial occurrence include autosomal recessive ... http://www.ncbi.nlm.nih.gov/pubmed/9489789   www.ncbi.nlm.nih.gov - summary OMIM Update List for December, 2003 114580 CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL DOMINANT ... 163000 NEVI FLAMMEI, FAMILIAL MULTIPLE ... 600430 BRACHYDACTYLY-MENTAL RETARDATION SYNDROME ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?12.2003   www.ncbi.nlm.nih.gov - summary OMIM Update List for March, 1999 113000 BRACHYDACTYLY, TYPE B1; BDB1. 120435 COLON CANCER, FAMILIAL NONPOLYPOSIS, TYPE 1 ... 143890 HYPERCHOLESTEROLEMIA, FAMILIAL; FHC ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?3.1999   www.ncbi.nlm.nih.gov - summary List of diseases (B) - Wikipedia, the free encyclopedia Benign familial infantile epilepsy. Benign fasciculation syndrome. Benign lymphoma ... Brachydactyly mesomelia mental retardation heart defects ... http://en.wikipedia.org/wiki/List_of_diseases_(B)   en.wikipedia.org - summary OMIM Update List for March, 2006 256450 HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 1; HHF1 ... 228900 FIBULAR HYPOPLASIA AND COMPLEX BRACHYDACTYLY. 266600 INFLAMMATORY BOWEL DISEASE 1; IBD1 ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?3.2006   www.ncbi.nlm.nih.gov - summary OMIM Update List for March, 2008 ... CONVULSIONS, FAMILIAL, 1; FEB1 ... for 151660 LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 2; FPLD2 ... SPONDYLOEPIPHYSEAL DYSPLASIA-BRACHYDACTYLY AND DISTINCTIVE ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?3.2008   www.ncbi.nlm.nih.gov - summary OMIM Update List for May, 1996 112410 BRACHYDACTYLY WITH HYPERTENSION. 120436 COLON CANCER, FAMILIAL, NONPOLYPOSIS TYPE 2 ... 176440 PREMATURE OVARIAN FAILURE, FAMILIAL; POF ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?5.1996   www.ncbi.nlm.nih.gov - summary List of diseases (F) - Wikipedia, the free encyclopedia Familial hyperlipoproteinemia type IV. Familial hyperlipoproteinemia ... Fibula aplasia complex brachydactyly. Fibular aplasia ectrodactyly ... http://en.wikipedia.org/wiki/List_of_diseases_(F)   en.wikipedia.org - summary OMIM Update List for April, 2000 267700 RETICULOSIS, FAMILIAL HISTIOCYTIC ... PARAGANGLIOMAS, FAMILIAL NONCHROMAFFIN, ... 112500 BRACHYDACTYLY, TYPE A1; BDA1. 114761 CARBONIC ANHYDRASE V; CA5A ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?4.2000   www.ncbi.nlm.nih.gov - summary OMIM Update List for April, 2002 ... for 140400 PROGRESSIVE FAMILIAL HEART BLOCK, TYPE ... 606835 DIGITAL ARTHROPATHY-BRACHYDACTYLY, FAMILIAL ... 120435 COLON CANCER, FAMILIAL NONPOLYPOSIS, TYPE 1 ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?4.2002   www.ncbi.nlm.nih.gov - summary List of diseases (H) - Wikipedia, the free encyclopedia Heart block progressive, familial. Heart block ... Hemangiomatosis, familial pulmonary ... Hypertrichosis brachydactyly obesity and mental retardation ... http://en.wikipedia.org/wiki/List_of_diseases_(H)   en.wikipedia.org - summary OMIM Update List for April, 2006 609968 HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 5; HHF5 ... 610023 BRACHYDACTYLY, COLOBOMA, AND ... 120400 COLOBOMA OF MACULA WITH TYPE B BRACHYDACTYLY ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?4.2006   www.ncbi.nlm.nih.gov - summary MIM Gene map Alport syndrome, autosomal recessive, 203780 (3); Hematuria,benign familial, 141200 (3) ... Brachydactyly-mental retardation syndrome (2) Ch. Copyright © 1966 ... http://www.ncbi.nlm.nih.gov/Omim/getmap.cgi?l147545   www.ncbi.nlm.nih.gov - summary MIM Gene map Alport syndrome, autosomal recessive, 203780 (3); Hematuria,benign familial, 141200 (3) ... Brachydactyly-mental retardation syndrome (2) Ch. 2q37. COL6A3 ... http://www.ncbi.nlm.nih.gov/Omim/getmap.cgi?l259900   www.ncbi.nlm.nih.gov - summary MIM Gene map ... deficiency, 231530 (3);Hyperinsulinemic hypoglycemia, familial, 4, 609975 (3) ... Brachydactyly, type A2, 112600 (3); Chrondrodysplasia, acromesomelic,with ... http://www.ncbi.nlm.nih.gov/Omim/getmap.cgi?l601609   www.ncbi.nlm.nih.gov - summary -- GeneReviews -- NCBI Bookshelf ... Hereditary Osteodystrophy-Like Syndrome, Brachydactyly-Mental Retardation ... Aceruloplasminemia Familial Apoceruloplasmin Deficiency, Hereditary ... http://www.ncbi.nlm.nih.gov/books/bv.fcgi?call=bv.View..ShowTOC&rid=gene.TOC   www.ncbi.nlm.nih.gov - summary Ectrodactyly - Wikipedia, the free encyclopedia Split hand and foot with familial occurrence" (in German) ... toes) · Arachnodactyly · Cenani Lenz syndactylism · Ectrodactyly · Brachydactyly ... http://en.wikipedia.org/wiki/Ectrodactyly   en.wikipedia.org - summary OMIM Update List for November, 1997 ... FEVER, FAMILIAL; MEFV ... 113100 BRACHYDACTYLY, TYPE C; BDC. 118945 CILIARY NEUROTROPHIC FACTOR; CNTF ... 601606 TRICHOEPITHELIOMA, MULTIPLE FAMILIAL ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?11.1997   www.ncbi.nlm.nih.gov - summary List of diseases (P) - Wikipedia, the free encyclopedia Paraplegia-brachydactyly-cone shaped epiphysis. Paraplegia-mental retardation-hyperkeratosis ... Polycystic ovarian disease, familial. Polycystic ovarian syndrome ... http://en.wikipedia.org/wiki/List_of_diseases_(P)   en.wikipedia.org - summary OMIM Update List for February, 1997 249100 MEDITERRANEAN FEVER, FAMILIAL; MEF ... 112410 BRACHYDACTYLY WITH HYPERTENSION. 123101 MSH (DROSOPHILA) HOMEO BOX HOMOLOG 2; MSX2 ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?2.1997   www.ncbi.nlm.nih.gov - summary CHOTZEN SYNDROME - Pedbase.org familial - autosomal dominant. chrom.#: 7p21. gene: ? M = F ? ... clinodactyly of the 5th finger and brachydactyly present. thumbs finger-like. 2. Toes ... http://pedbase.org/c/chotzen-syndrome/   pedbase.org - summary OMIM Update List for June, 2004 606415 CANDIDIASIS, FAMILIAL CHRONIC MUCOCUTANEOUS, AUTOSOMAL DOMINANT, WITH ... 112410 HYPERTENSION WITH BRACHYDACTYLY. 116955 ZINC FINGER PROTEIN 9; ZNF9 ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?6.2004   www.ncbi.nlm.nih.gov - summary MIM Gene map Cardiomyopathy, familial hypertrophic, 9 (3); Cardiomyopathy,dilated, 1G, 604145 ... (3); Syndactyly, type V, 186300 (3); Brachydactyly-syndactyly syndrome,610713 (3) ... http://www.ncbi.nlm.nih.gov/Omim/getmap.cgi?l606708   www.ncbi.nlm.nih.gov - summary 2q37 Deletion Syndrome -- GeneReviews -- NCBI Bookshelf Familial chromosome rearrangements have been identified in approximately 5% of ... The critical region for brachydactyly has been mapped to HDAC proximally and ... http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=del2q37.2   www.ncbi.nlm.nih.gov - summary Holt-Oram Syndrome -- GeneReviews -- NCBI Bookshelf Familial progressive sinoatrial and atrioventricular conduction disease of adult ... including Holt-Oram syndrome, ulnar-mammary syndrome, brachydactyly type B and ... http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=hos   www.ncbi.nlm.nih.gov - summary Julia Bell - Wikipedia, the free encyclopedia ... Bell did pioneering work in documenting the familial nature of many diseases. ... X syndrome, Julia Bell's name is associated with five forms of brachydactyly. ... http://en.wikipedia.org/wiki/Julia_Bell   en.wikipedia.org - summary List of diseases (C) - Wikipedia, the free encyclopedia Cardiac conduction defect, familial. Cardiac diverticulum ... Coloboma of macula type B brachydactyly. Coloboma of macula. Coloboma of optic nerve ... http://en.wikipedia.org/wiki/List_of_diseases_(C)   en.wikipedia.org - summary OMIM Update List for October, 2002 113100 BRACHYDACTYLY, TYPE C; BDC. 116806 CATENIN, BETA-1; CTNNB1 ... 602347 CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 3 ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?10.2002   www.ncbi.nlm.nih.gov - summary OMIM Update List for December, 1998 603373 HYPERTHYROIDISM, FAMILIAL GESTATIONAL ... 600430 BRACHYDACTYLY-MENTAL RETARDATION SYNDROME ... 120435 COLON CANCER, FAMILIAL, NONPOLYPOSIS TYPE 1 ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?12.1998   www.ncbi.nlm.nih.gov - summary List of diseases (E) - Wikipedia, the free encyclopedia Exostoses anetodermia brachydactyly type E. Exostoses, multiple, type 1 ... Exudative retinopathy familial, autosomal dominant ... http://en.wikipedia.org/wiki/List_of_diseases_(E)   en.wikipedia.org - summary OMIM Update List for December, 2008 612422 CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3; RCM3 ... 113300 BRACHYDACTYLY, TYPE E; BDE ... Clinical Synopsis for 600430 BRACHYDACTYLY-MENTAL RETARDATION SYNDROME ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?12.2008   www.ncbi.nlm.nih.gov - summary OMIM Update List for March, 1997 120436 COLON CANCER, FAMILIAL, NONPOLYPOSIS TYPE 2 ... 112410 BRACHYDACTYLY WITH HYPERTENSION. 123660 CRYSTALLIN, GAMMA A; CRYGA ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?3.1997   www.ncbi.nlm.nih.gov - summary OMIM Update List for March, 2005 Clinical Synopsis for 193007 VESTIBULOPATHY, FAMILIAL ... 113000 BRACHYDACTYLY, TYPE B1; BDB1. 127500 DYSCHROMATOSIS UNIVERSALIS HEREDITARIA ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?3.2005   www.ncbi.nlm.nih.gov - summary OMIM Update List for August, 2001 120435 COLON CANCER, FAMILIAL NONPOLYPOSIS, TYPE 1 ... 186550 SYNOSTOSIS, CARPAL, WITH DYSPLASTIC ELBOW JOINTS AND BRACHYDACTYLY ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?8.2001   www.ncbi.nlm.nih.gov - summary Macrocephaly - Wikipedia, the free encyclopedia ... with macrocephaly, including familial macrocephaly, autism, PTEN mutations ... toes) · Arachnodactyly · Cenani Lenz syndactylism · Ectrodactyly · Brachydactyly ... http://en.wikipedia.org/wiki/Macrocephaly   en.wikipedia.org - summary MIM Gene map Brachydactyly, type A2, 112600 (3); Chrondrodysplasia, acromesomelic,with ... {Atrial fibrillation, familial, 5} (2) association with rs2200733 and rs10033464. Fd ... http://www.ncbi.nlm.nih.gov/Omim/getmap.cgi?l611065   www.ncbi.nlm.nih.gov - summary List of diseases (M) - Wikipedia, the free encyclopedia Metaphyseal dysplasia maxillary hypoplasia brachydactyly. Metaphyseal dysplasia Pyle type ... Multiple fibrofolliculoma familial. Multiple hereditary exostoses ... http://en.wikipedia.org/wiki/List_of_diseases_(M)   en.wikipedia.org - summary OMIM Update List for October, 1996 113100 BRACHYDACTYLY, TYPE C. 114182 CALMODULIN 2; CALM2. 114183 CALMODULIN 3; CALM3 ... 141200 HEMATURIA, BENIGN FAMILIAL; BFH ... http://www.ncbi.nlm.nih.gov/Omim/dispmonthly.cgi?10.1996   www.ncbi.nlm.nih.gov - summary List of diseases (T) - Wikipedia, the free encyclopedia Temporal epilepsy, familial. Temporomandibular ankylosis ... Thumb stiff brachydactyly mental retardation [edit] Thy. Thymic carcinoma ... http://en.wikipedia.org/wiki/List_of_diseases_(T)   en.wikipedia.org - summary show more 1  2