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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 22 found (95 total)

alternate case: ectrodactyly

SHFM3P1 (368 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 (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 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 (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:10

List 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 paralysis

Microphthalmia (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 (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 (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 Holoprosencephaly

Pili torti (4,439 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 syndrome

TLX (936 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

Chromosome 3 (1,991 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–Hailey

List of diseases (C) (3,657 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

List of diseases (B) (1,049 words) [view diff] exact match in snippet view article

Blepharophimosis Blepharoptosis aortic anomaly Blepharoptosis cleft palate ectrodactyly dental anomalies Blepharoptosis-myopia-ectopia lentis Blepharospasm

Keratinocyte (2,756 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

Loose anagen syndrome (2,469 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

Adams–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 474617

List 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 syndrome

List of diseases (S) (1,933 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) (2,469 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 unusual

The Wizard of Paws (333 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 prosthetic

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;