34 Matching Annotations
- May 2022
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watermark.silverchair.com watermark.silverchair.com
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DICER1 syndrome is an autosomal-dominant,pleiotropic, tumor-predisposition disorder arisingfrom pathogenic germline variants in DICER1, whichencodes an endoribonuclease integral to processingmicroRNAs
DICER1 is the gene name. PubMed ID, HGCNCID, and Variant: I can't find Inheritance Pattern: autosomal-dominant The disease entity: DICER1 syndrome The type of mutation: germline. Zygosity: not known. Family Information: a family was used, DICER1 carriers, and non DICER1 variant used, some of the family members had tumors from DICER1 Case Information: mean age is 34, the range of age is 18.6 to 43 years, male, and female used, ethnicity can't find Case Presenting HPO: cancer testing, chemotherapy, radiotherapy gnomeAD: 9.2,8.3.2 Mutation type: Pleiotropic, loss of function, missense
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- Dec 2019
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academic.oup.com academic.oup.com
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average stature
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average stature
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average stature
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average stature
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average stature
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average stature
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average stature
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average stature
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Height
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average-stature
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average stature
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- Oct 2019
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Local file Local file
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cryptorchidism on the right side.
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- Sep 2019
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www.sciencedirect.com www.sciencedirect.com
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complete destruction of carpal bones
HP:0001495
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- Aug 2019
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link.springer.com link.springer.com
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autism spectrum disorder
HP_0000729,DOID_2030,HP_0000739,ZP_0005531,SO_1000039
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ASDs are frequently associated with comorbid intellectual disability (ID), ranging between 30 and 60% of cases depending on the sampling methods and measurements used
DOID_12849,HP_0000717
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ASDs are frequently associated with comorbid intellectual disability (ID), ranging between 30 and 60% of cases depending on the sampling methods and measurements used
- obsolete Peripheral visual field constriction with 30-39 degrees central field preserved
- mixed embryonal carcinoma and endodermal sinus neoplasm with seminoma of the testis
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hypothes.is hypothes.is
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using the sidebar on the ri
HP_0031638,HP_0011605
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hypothes.is hypothes.is
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nd running. It's time to start annotati
- obsolete Acral ulceration and osteomyelitis leading to autoamputation of the digits (feet)
- Combined hamartoma of the retinal pigment epithelium and retina
- sex-limited autosomal dominant inheritance
- sex-limited autosomal recessive inheritance
- Postoperative
- OperationHistory
- MedicationHistory
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- Jul 2019
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hypothes.is hypothes.is
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e! Enable the sidebar via the button in the location bar.
- Ulnar deviation of the 4th finger
- Ulnar deviation of the hand or of fingers of the hand
- Ulnar deviation of the 5th finger
- MedicationforEuthanasia
- AntineoplaticDrugAgentTherapy
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Try it on this sentence.
- Double outlet right ventricle with non-committed ventricular septal defect and pulmonary stenosis
- Double outlet right ventricle with subpulmonary ventricular septal defect without pulmonary stenosis
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hypothes.is hypothes.is
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- Partial duplication of the middle phalanges of the hand
- Partial duplication of the middle phalanx of the 2nd toe
- Partial duplication of the middle phalanx of the 4th finger
- Partial duplication of the middle phalanx of the 2nd finger
- heteroplasmic mitochondrial inheritance
- sequence_length_variation
- sex-limited autosomal dominant inheritance
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hypothes.is hypothes.is
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otate! Enable the sidebar via the button in the location bar.
- Ulnar deviation of the 4th finger
- Ulnar deviation of the 5th finger
- Supraventricular tachycardia with a concealed accessory pathway on the right free wall
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hypothes.is hypothes.is
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annotate! Enable the sidebar via the button in the location bar.
- Triangular shaped proximal phalanx of the 4th finger
- separation anxiety disorder
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hypothes.is hypothes.is
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tate! Enable the sidebar via the button in the location bar.
- Ulnar deviation of the 4th finger
- Ulnar deviation of the 5th finger
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hypothes.is hypothes.is
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Go forth and annotate! Enable the sidebar via the button in the location bar
- Partial duplication of the middle phalanx of the 4th finger
- Partial duplication of the middle phalanx of the 5th finger
- Rare_or_No_Social_Approaches_of_Showing_and_Directing_Attention
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hypothes.is hypothes.is
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idebar via the button in the location bar.
- Ulnar deviation of the 4th finger
- Ulnar deviation of the 5th finger
- sequence_length_variation
- heteroplasmic mitochondrial inheritance
- Definite_unusual_and_marked_resistance_to_trivial_changes_in_the_environment
- Spontaneous_imitation_limited_to_a_few_familiar_routines_that_are_not_incorporated_into_play
- One_or_More_Relationships_That_Involve_Some_Personal_Shared_Activities
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hypothes.is hypothes.is
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at can be created with the applicatio
- Dense calcifications in the cerebellar dentate nucleus
- Disorganization of the anterior cerebellar vermis
- MedicationforNutrition
- OccupationalTherapy
- Speech_tendsOrTended_to_be_more_repetitive_than_most_subject
- One_or_more_activities_that_subject_has_to_preform_in_a_special_way_if_disrupted_appears_to_be_under_MARKED_pressure
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- Jun 2019
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europepmc.org europepmc.org
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Nonsyndromic intellectual disability
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- May 2019
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Local file Local file
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Enlarged ventricles
ventriculomegaly
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ituitarystalk hypoplasi
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general or cortical atrophy
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neuronal migration defect
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enlarged cisterna magna
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