Disease Comparison Results (show all mode) for Cryptophthalmos (Fraser) syndrome and Dysplastic Nevus Syndrome, Familal

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Dysplastic Nevus Syndrome, Familal

Found: 17 | Differences: 16

Cryptophthalmos (Fraser) syndrome

Found: 80 | Differences: 79

Cryptophthalmos (Fraser) syndrome and Dysplastic Nevus Syndrome, Familal sharing one common finding. (show all, show common, show differences)

Clinical Manifestations
Signs & Symptoms
Brown skin discoloration
Increased pigmentation/tanning/hyperpigmented
Pigmentation Lesions on Healing
Pigmented patches/skin
Associated Diseases & Rule outs
Associated Disease & Complications - Rule Outs
Melanoma, malignant
Associated Disease & Complications - Causes
Congenital nevus
Familial atypical mole syndrome
Hyperpigmentation
Melanoma, malignant
Disease Mechanism & Classification
Class
CLASS/Dermatologic/Subcutaneous (category)
Process
PROCESS/Dysplasia/aplasia (ex)
PROCESS/Hereditofamilial (category)
PROCESS/Hereditofamilial/tumor syndrome (ex)
PROCESS/Neoplastic (category)
PROCESS/Pre-Malignant condition (ex)
PROCESS/Dysplasia disorder/Syndromes (ex)
Synonyms
Synonym
Synonym/Dysplastic nevus syndrome
Clinical Manifestations
Signs & Symptoms
Congenital low hairline
Particular physiognomy/Odd looking kids
Craniofacial Abnormalities/Congenital
Facies particular
Genital Hypoplasia/Male
Penis, small (Micropenis)
Uvula anomaly/deformity
Webbed fingers
Intelligence normal
Mental Deficiency Child
Clitoral enlargement
Clitoral enlargement/newborn
Congenital absent eyes/palpebral fissures
Narrow Palpebral Fissures
Anomalous ears/deformities
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
Sex & Age Groups
Population/Child
Population/Child-Infant Only
Population/Children/all
Population/Infant
Associated Diseases & Rule outs
Associated Disease & Complications
Anal Atresia
Blindness
Cleft Lip
Cleft lip/deformity
Cleft palate/deformity
Congenital anomalies
Congenital heart disease
Congenital urinary tract malformations
Cryptophthalmos syndrome
Cryptorchidism
Deafness
Facial dysplasia
Fetal anomaly
Hypospadius anomaly
Imperforate anus
Labial fusion/infant
Laryngostenosis
Limb deformities/anomalies
Meningoencephalocele
Meningomyelocele
Mental retardation
Microphallus deformity
Microphthalmos
Multiple Congenital Anomalies
Multiple congenital anomalies/Mental retardation
Renal anomaly/aplasia/hypoplasia
Syndactyly/Webbing
Uterus Didelphus/Bicornuate
Genital Hypoplasia
Hand anomalies
Disease Mechanism & Classification
Class
CLASS/Jablonski/NIH Archive Anomalies Database
CLASS/Pediatric disorders (ex)
CLASS/Eye involvement/disorder (ex)
CLASS/Globe (eye) disorder (ex)
Pathophysiology
Pathophysiology/Gene locus 4q21
Pathophysiology/Gene Locus Identified/OMIM database
Pathophysiology/Gene locus/Chromosome 4
Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
Pathophysiology/Maternal Chromosome mutation
Pathophysiology/Palpebral absence/Eye/Globes present
Process
PROCESS/Autosomal recessive disorder (ex)
PROCESS/Congenital/developmental (category)
PROCESS/Eponymic (category)
PROCESS/Genetic disorder/Spontaneous mutations/sporadic
PROCESS/Hereditofamilial (category)
PROCESS/INCIDENCE/Rare disease (ex)
PROCESS/Multiple dysmorphic syndrome (ex)
PROCESS/Anomalies/Deformities/Malformations (EX)
PROCESS/Dystostosis/craniofacial (ex)
PROCESS/Congenital eye disorder (ex)
Synonyms
Synonym
Synonym/Cryptophthalmos-Syndactyly Syndrome
Synonym/Fraser-Francois Syndrome
Synonym/Fraser's syndrome
Treatment
Drug Therapy
SX/Eye Surgery
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