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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), Anonychia-onychodystrophy with brachydactyly type B and ectrodactyly (view), Intellectual disability-spasticity-ectrodactyly syndrome (view), Fibular aplasia-ectrodactyly syndrome (view), Triphalangeal thumbs-brachyectrodactyly syndrome (view)

searching for Ectrodactyly 20 found (88 total)

alternate case: ectrodactyly

SHFM3P1 (360 words) [view diff] exact match in snippet view article find links to article

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 (289 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 incisor
SHFM1 (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 CJ
SNX3 (577 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:10
List 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–Calzolari
List of diseases (T) (845 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 paralysis
Microphthalmia (2,192 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:10.1136/jmg
List of diseases (H) (1,727 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 Holoprosencephaly
TLX (935 words) [view diff] exact match in snippet view article find links to article
NR2E1 and SNX3 in five patients with MMEP (microcephaly, microphthalmia, ectrodactyly, and prognathism) and related phenotypes". BMC Medical Genetics. 8: 48
List of diseases (C) (3,634 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 mental
Keratinocyte (2,729 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 transcriptome
List of diseases (B) (1,031 words) [view diff] exact match in snippet view article
Blepharophimosis Blepharoptosis aortic anomaly Blepharoptosis cleft palate ectrodactyly dental anomalies Blepharoptosis myopia ectopia lentis Blepharospasm
Loose 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, Trichorhinophalangeal
List of diseases (A) (1,927 words) [view diff] exact match in snippet view article
pancreas Annuloaortic ectasia Anodontia Anomic aphasia Anonychia Anonychia ectrodactyly Anonychia microcephaly Anonychia onychodystrophy Anonychia onychodystrophy
Adams–Oliver syndrome (1,943 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 474617
List of diseases (P) (1,910 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 syndrome
List of diseases (S) (1,929 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 stature
Hecht 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/ajmg
List of diseases (M) (2,464 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 unusual
List 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;