Disease Comparison Results (show all mode) for Hemoglobin M disease and Hypothalamic hypogonadism, Kallman's

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Hypothalamic hypogonadism, Kallman's

Found: 113 | Differences: 104

Hemoglobin M disease

Found: 13 | Differences: 4

Hemoglobin M disease and Hypothalamic hypogonadism, Kallman's sharing 9 common findings. (show all, show common, show differences)

Clinical Manifestations
Signs & Symptoms
Particular physiognomy/Odd looking kids
Craniofacial Abnormalities/Congenital
Breast Swelling Bilateral
High blood pressure child
Delayed male adolescence/pubescence
Genital Hypoplasia/Male
Penile deformity
Penis, small (Micropenis)
Small testes
Testes/small firm
Appetite increased
Polyphagia
Uvula anomaly/deformity
Webbed fingers
Mental Deficiency Child
Amenorrhea
Amenorrhea, primary
Amenorrhea, secondary
Anosmia/Loss of sense of smell
Decreased sense of smell
Tall Adult
Weight gain
Color blindness acquired/dimming
Clinical Presentation & Variations
Presentation/Multiple deformities newborn (odd look)
Disease Progression
Course/Chronic disorder
Course/Chronic only
Demographics & Risk Factors
Population Group
Child
Infant
Population/Pediatrics population
Family History
Family history/Skeletal malformations
Sex & Age Groups
Population/Boy patient
Population/Child
Population/Child-Infant Only
Population/Children/all
Population/Infant
Population/Male
Laboratory Tests
Abnormal Lab Findings (Non Measured)
DNATest specific/genetics laboratory/abnormality (Lab)
FSH/LH Ratio (Lab)
Abnormal Lab Findings - Decreased
FSH/Follicle Stmulating Hormone/ICSH (Lab)
LH/Leutinizing Hormone (Lab)
Testosterone Total (Lab)
URINE FSH
URINE Leutininzing hormone
Diagnostic Test Results
X-RAY
Xray/Delayed bone age/slow epiphysis closures
Xray/Hand short fourth metacarpal bone
Associated Diseases & Rule outs
Associated Disease & Complications - Rule Outs
Congenital heart disease
Associated Disease & Complications - Causes
Cleft Lip
Cleft lip/deformity
Cleft palate/deformity
Color blind
Congenital anomalies
Congenital heart disease
Deafness
Deafness, congenital
Deafness, sensorineural
Facial dysplasia
Gonadotropin deficiency/Female acquired
Gut Anomalies
Gynecomastia
Hypertension
Hypertension in a child
Hypogonadism, male
Hypothalamic defect/Kallman's syndrome
Hypothalamic dysfunction
Intestine malrotation
Limb deformities/anomalies
Mental retardation
Multiple Congenital Anomalies
Multiple congenital anomalies/Mental retardation
Obesity
Obesity in Children
Ovarian Dysfunction
Panhypopituitarism
Secondary female hypogonadism
Secondary male hypogonadism
Skeletal dysplasia
Skeletal/bone malformations
Syndactyly/Webbing
Hand anomalies
Metacarpal Anomalies
Disease Mechanism & Classification
Class
CLASS/Jablonski/NIH Archive Anomalies Database
CLASS/Pediatric disorders (ex)
CLASS/Endocrine gland (category)
CLASS/Hypothalamus/neurohypophysis involvement (ex)
CLASS/Neurologic (category)
Pathophysiology
Pathophysiology/Gene locus 8p11.2-p11.1
Pathophysiology/Gene Locus Identified/OMIM database
Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
Pathophysiology/Gonadotrophic releasing hormone/defect
Pathophysiology/Hypogonadotrophic hypogonadism
Pathophysiology/Secondary Testicular Failure
Pathophysiology/Sperm Production Decreased
Pathophysiology/Ovarian dysfunction anovulation
Pathophysiology/Maternal Chromosome mutation
Pathophysiology/Gene locus chromosome 8
Process
PROCESS/Autosomal dominant hereditary disease (ex).
PROCESS/Congenital/developmental (category)
PROCESS/Endocrine/humoral disorders (category)
PROCESS/Eponymic (category)
PROCESS/Genetic disorder/Spontaneous mutations/sporadic
PROCESS/Hereditofamilial (category)
PROCESS/INCIDENCE/Rare disease (ex)
PROCESS/Hypogonadotropic hypogonadism/congenital
PROCESS/Congenital CNS disorder (ex)
PROCESS/Dystostosis/craniofacial (ex)
Synonyms
Synonym
Synonym/Hypogonadotropic hypogonadism/anosmia male
Synonym/Kallman syndrome
Clinical Manifestations
Disease Progression
Course/Chronic disorder
Course/Chronic only
Demographics & Risk Factors
Population Group
Child
Population/Pediatrics population
Sex & Age Groups
Population/Child
Population/Child-Infant Only
Population/Children/all
Laboratory Tests
Abnormal Lab Findings (Non Measured)
Hemoglobin electrophoresis abnormal (Lab)
Disease Mechanism & Classification
Class
CLASS/Hematologic (category)
Pathophysiology
Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
Process
PROCESS/Hereditofamilial (category)
PROCESS/Hemoglobinopathy disorder (ex)
PROCESS/Molecular/hematologic disorder (ex)
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