Differential Diagnosis
Diseases
Drugs
More
[+] Tips
- Try building your search one term at a time, and be as specific as you can! Search term example: "chronic cough".
- Do not enter multiple findings such as "anemia, chronic cough, weight loss, vomiting" all at the same time.
- After selecting your term from the search results a list of possible diagnoses will be generated. If the list is too long, you will be able to narrow it down by entering additional terms.
- Do not enter values such as "heart rhythm 110" or "sodium 125", instead use "tachycardia" or "hyponatremia".

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

Clinical
Demographics
Lab
Diagnostic
Diseases
Classification
Synonyms
Start Over

Found: 113 | Differences: 104

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)

Ads

This site is designed primarily as a reminder system for use by qualified physicians and other medical professionals. By using this site you understand and accept that DiagnosisPro.com shall not be used as a diagnostic decision-making system and must not be used to make a clinical diagnosis or replace or overrule a licensed health care professional's judgment or clinical diagnosis (full terms of use). This site complies with the HONcode standard for trustworthy health information: verify here.