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Find link is a tool written by Edward Betts.Longer titles found: Ectrodactyly-polydactyly syndrome (view), Ectrodactyly with tibia aplasia/hypoplasia (view), Ectrodactyly–ectodermal dysplasia–cleft syndrome (view), Holoprosencephaly-ectrodactyly-cleft lip/palate syndrome (view), Intellectual disability-spasticity-ectrodactyly syndrome (view), Anonychia-onychodystrophy with brachydactyly type B and ectrodactyly (view), Fibular aplasia-ectrodactyly syndrome (view), Triphalangeal thumbs-brachyectrodactyly syndrome (view)
searching for Ectrodactyly 22 found (93 total)
alternate case: ectrodactyly
SHFM3P1
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Split hand/foot malformation (ectrodactyly) type 3 pseudogene 1, also known as SHFM3P1, is a human gene. GRCh38: Ensembl release 89: ENSG00000230701 –Weyer's ulnar ray/oligodactyly syndrome (292 words) [view diff] exact match in snippet view article find links to article
is a rare multi-systemic genetic disorder which is characterized by ectrodactyly, ulnar, radial, or fibular ray deficit, and heart, single central incisorSHFM1 (840 words) [view diff] exact match in snippet view article find links to article
571. PMID 8733122. "Entrez Gene: SHFM1 split hand/foot malformation (ectrodactyly) type 1". Marston NJ, Richards WJ, Hughes D, Bertwistle D, Marshall CJSNX3 (580 words) [view diff] exact match in snippet view article find links to article
with a translocation t(6;13)(q21;q12) and microcephaly, microphthalmia, ectrodactyly, prognathism (MMEP) phenotype". J. Med. Genet. 39 (12): 893–9. doi:10List of diseases (F) (924 words) [view diff] exact match in snippet view article
arousal disorder Femoral facial syndrome Femur bifid with monodactylous ectrodactyly Femur fibula ulna syndrome Fenton–Wilkinson–Toselano syndrome Ferlini–Ragno–CalzolariList of diseases (T) (849 words) [view diff] exact match in snippet view article
radial anomalies osteopenia fracture Tibial aplasia ectrodactyly hydrocephalus Tibial aplasia ectrodactyly Tibial hemimelia cleft lip palate Tick paralysisMicrophthalmia (2,173 words) [view diff] exact match in snippet view article find links to article
with a translocation t(6;13)(q21;q12) and microcephaly, microphthalmia, ectrodactyly, prognathism (MMEP) phenotype". Journal of Medical Genetics. 39 (12):List of diseases (H) (1,717 words) [view diff] exact match in snippet view article
Holoprosencephaly caudal dysgenesis Holoprosencephaly deletion 2p Holoprosencephaly ectrodactyly cleft lip palate Holoprosencephaly radial heart renal anomalies HoloprosencephalyPili torti (4,454 words) [view diff] exact match in snippet view article find links to article
dysplasia 4, hair/nail type, ectodermal dysplasia with corkscrew hairs, ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3, Goltz syndromeList of diseases (C) (3,648 words) [view diff] exact match in snippet view article
sacral lipoma Cleft lip palate dysmorphism Kumar type Cleft lip palate ectrodactyly Cleft lip palate incisor and finger anomalies Cleft lip palate mentalChromosome 3 (1,978 words) [view diff] exact match in snippet view article find links to article
epidermolysis bullosa Endplate acetylcholinesterase deficiency Essential tremors Ectrodactyly, Case 4 Glaucoma, primary open angle Glycogen storage disease Hailey–HaileyKeratinocyte (2,752 words) [view diff] exact match in snippet view article find links to article
keratinocytes. Mutations in the p63 DNA-binding domain are associated with ectrodactyly, ectodermal dysplasia, and cleft lip/palate (EEC) syndrome. The transcriptomeList of diseases (B) (1,032 words) [view diff] exact match in snippet view article
Blepharophimosis Blepharoptosis aortic anomaly Blepharoptosis cleft palate ectrodactyly dental anomalies Blepharoptosis-myopia-ectopia lentis BlepharospasmList of diseases (A) (1,929 words) [view diff] exact match in snippet view article
pancreas Annuloaortic ectasia Anodontia Anomic aphasia Anonychia Anonychia ectrodactyly Anonychia microcephaly Anonychia onychodystrophy Anonychia onychodystrophyLoose anagen syndrome (2,465 words) [view diff] exact match in snippet view article find links to article
include; Coloboma, Noonan syndrome, Hypohidrotic ectodermal dysplasia, EEC (ectrodactyly- ectodermal dysplasia-clefting) syndrome, Neurofibromatosis, TrichorhinophalangealAdams–Oliver syndrome (1,952 words) [view diff] exact match in snippet view article find links to article
Beighton P (1979). "Autosomal dominant inheritance of scalp defects with ectrodactyly". Am J Med Genet. 3 (1): 35–41. doi:10.1002/ajmg.1320030109. PMID 474617Hecht Scott syndrome (936 words) [view diff] exact match in snippet view article find links to article
Reed, Martin H.; Greenberg, Cheryl H. (2002). "Fibular aplasia with ectrodactyly". American Journal of Medical Genetics. 113 (1): 52–58. doi:10.1002/ajmgList of diseases (S) (1,934 words) [view diff] exact match in snippet view article
Short stature microcephaly seizures deafness Short stature monodactylous ectrodactyly cleft palate Short stature prognathism short femoral necks Short statureList of diseases (P) (1,908 words) [view diff] exact match in snippet view article
chronic myeloid leukemia Phocomelia contractures absent thumb Phocomelia ectrodactyly deafness sinus arrhythmia Phocomelia Schinzel type Phocomelia syndromeList of diseases (M) (2,469 words) [view diff] exact match in snippet view article
Mental retardation Smith–Fineman–Myers type Mental retardation spasticity ectrodactyly Mental retardation u – Mental retardation x Mental retardation unusualThe Wizard of Paws (331 words) [view diff] exact match in snippet view article find links to article
going to help the Sotnik family's Corgi, Ollie, born with split-paw ectrodactyly. The shorter legs and lack of a pronounced elbow to anchor a prostheticList of OMIM disorder codes (18,877 words) [view diff] exact match in snippet view article find links to article
Ectodermal dysplasia, anhidrotic, X-linked; 305100; ED1 Ectodermal dysplasia, ectrodactyly, and macular dystrophy; 225280; CDH3 Ectodermal dysplasia, hidrotic;