Disease Comparison Results (show all mode) for Cowden disease/CD (10q23.31) and Rh-Null syndrome

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Rh-Null syndrome

Found: 19 | Differences: 16

Cowden disease/CD (10q23.31)

Found: 82 | Differences: 79

Cowden disease/CD (10q23.31) and Rh-Null syndrome sharing 3 common findings. (show all, show common, show differences)

Clinical Manifestations
Clinical Presentation & Variations
Anemia in Children
Demographics & Risk Factors
Sex & Age Groups
Population/Child
Laboratory Tests
Abnormal Lab Findings (Non Measured)
Stomatocytosis on Differential smear (Lab)
Abnormal Lab Findings
Osmotic fragility, RBC (Lab)
Spherocytes (Lab)
Associated Diseases & Rule outs
Associated Disease & Complications
Anemia
Hemolytic anemia, congenital
Spherocytosis, acquired
Disease Mechanism & Classification
Class
CLASS/Erythrocyte disorder (ex)
CLASS/Hematologic (category)
CLASS/Intrinsic RBC abnormality (ex)
Pathophysiology
Pathophysiolog/RBC Passive Membrane Leak Excess
Pathophysiology/Maternal Chromosome mutation
Process
PROCESS/Autosomal dominant hereditary disease (ex).
PROCESS/Autosomal recessive disorder (ex)
PROCESS/Genetic disorder/Spontaneous mutations/sporadic
PROCESS/Hereditofamilial (category)
PROCESS/INCIDENCE/Rare disease (ex)
Clinical Manifestations
Signs & Symptoms
Facies/Bird like
Sunken Cheek Bones
Breast Swelling Bilateral
Virginal Breast Hyperplasia
Multiple facial papules
Palmar keratosis
Skin tags/papillomata/increased sudden new growth
Cobblestone papules gingiva/buccal mucosa
High arched palate
Hypoplasia Narrow Maxilla
Narrow oral aperture/small mouth opening
Oral papillomas
Receding chin deformity
Scrotal Tongue deformity
Action Tremor
Mental Deficiency Child
Progressive macrocephaly/infant/sign
Tremor,intention
Ovary mass
Psychomotor retardation
Sternum deformities
Snoring
Clinical Presentation & Variations
Presentation/Breast Carcinoma Young Woman
Associated Diseases & Rule outs
Associated Disease & Complications - Rule Outs
Gardner syndrome
Associated Disease & Complications - Causes
Acute Myelogenous/Myeloblastic Leukemia AML
Adenocarcinoma, breast
Adenocarcinoma, ovary
Adenocarcinoma, uterus
Bladder polyp
Breast fibroadenoma
Breast fibrocystic disease
Breast hamartoma
Carcinoma, bladder, transitional
Cerebellar Gangliocytoma
Cerebellar tumor
Cervix carcinoma
Colon polyp
Diverticulosis, colon
Goiter simple/non-endemic
Gynecomastia
Hydrocele cord
Hyperthyroidism (Graves disease)
Hypothyroidism (myxedema)
Kyphoscoliosis
Kyphosis
Lipoma
Mandible hypoplasia/Retrognathia
Megaloencephaly
Meningioma
Mental retardation
Micrognathia/congenital small chin
Multiple hamartoma syndrome
Ovarian cyst
Pectus excavatum
Plantar callous/palmar callous keratosis
Thyroid adenoma
Thyroid follicular adenoma
Thyroid papillary carcinoma
Uterine fibroid/leiomyomas
Vaginal cyst
Varicocele
Vulva Cyst
Facial Trichilemmomas
Disease Mechanism & Classification
Class
CLASS/Pediatric disorders (ex)
Pathophysiology
Pathophysiology/Anticipation kindred inheritance earlier onset effect
Pathophysiology/Gene locus 10q22.3
Pathophysiology/Gene locus 10q23.31
Pathophysiology/Gene locus Chromosome 10
Pathophysiology/Gene Locus Identified/OMIM database
Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
Pathophysiology/Hereditary Cancer
Pathophysiology/Maternal Chromosome mutation
Pathophysiology/Mutation BMPRIA gene
Pathophysiology/PTEN homolog gene mutation
Process
PROCESS/Autosomal dominant hereditary disease (ex).
PROCESS/Eponymic (category)
PROCESS/Eponymic/Esoteric/Not yet integrated into database
PROCESS/Genetic disorder/Spontaneous mutations/sporadic
PROCESS/Hamartoma type neoplasm (ex)
PROCESS/Hereditary Multiple anomalies syndrome [EX]
PROCESS/Phakomatosis/congenital (ex)
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