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- Disease Information
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Disease Processes ▼
- Auto Immune
- Vascular-Arteriosclerosis
- Biochemical
- Congenital-developmental
- Deficiency
- Degenrative-Necrosis
- Electromagnetic-Physics
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- Functional-Physiologic
- Hereditofamilial
- Iatrogenic
- Idiopathic
- Infected Organ-Abcess
- Infectious agent
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- Metabolic-Storage
- Neoplastic
- Poison Agent
- Poisoned Organ
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- Trauma
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Major Organs-Systems ▼
- Systemic
- Pediatric
- Nervous & Sensory System (Neurology)
- Cardiovascular System
- Respiratory (Pulmonary) System
- Gastro-Intestinal (Digestive) System
- Urinary System
- Dermatologic System
- Endocrine System
- Immune System
- Musculoskeletal System
- Genital Reproductive System
- Hematopoietic System (Hematology)
- Lymphatic System
- Tissue/Cells/Organelles
Disease Comparison Results (show differences mode) for C/D chromosome translocation and Incontinentia pigmenti/hereditary
Incontinentia pigmenti/hereditary
Found: 65 | Differences: 56
Found: 14 | Differences: 5
C/D chromosome translocation and Incontinentia pigmenti/hereditary sharing 9 common findings. (show all, show common, show differences)
- Clinical Manifestations
- Signs & Symptoms
- Birthmark
- Decreased sweating/Absent sweating
- Face skin lesions
- Fissuring palms/soles
- Hyperkeratosis/palms and soles
- Increased pigmentation/tanning/hyperpigmented
- Reticular pigmentations
- Slate gray pigmentations
- Small nails/congenital
- Vesicobullous rash/lesions in Children
- Vesicobullous rashes
- Carious teeth/child
- Carious teeth/sign
- Dental/enamel erosion/discoloration
- Teeth malformed/dysplastic
- Tooth Enamel defects
- Yellowing teeth
- Autonomic instability/Variable BP/HR
- Infant Seizures
- Mental Deficiency Child
- Seizures
- Seizures/Children/recurrent
- Macrocephaly/Large head
- Megalocephaly
- Blue Sclera
- Disease Progression
- Course/Progressive
- Course/Progressive/slowly chronic illness
- Onset/Infancy
- Onset/insidious
- Demographics & Risk Factors
- Population Group
- Infant
- Sex & Age Groups
- Population/Infant
- Associated Diseases & Rule outs
- Associated Disease & Complications
- Anhydrosis/Absent sweating/diffuse
- Dental caries
- Dental deformities/anomalies
- Fetal wastage
- Hyperpigmentation
- Incontenintia pigmenti/hereditary
- Mental retardation
- Microcephaly/oligophrenia
- Teeth enamel hypoplastic
- Vasomotor instability
- Disease Mechanism & Classification
- Class
- CLASS/Pediatric disorders (ex)
- CLASS/Dermatologic/Subcutaneous (category)
- Pathophysiology
- Pathophysiology/Homozygous/dominant lethal
- Pathophysiology/X-linked dominant allele/Heterozygous
- Pathophysiology/Lethal Mutation Homozygous
- Process
- PROCESS/Autosomal dominant hereditary disease (ex).
- PROCESS/Phakomatosis/congenital (ex)
- PROCESS/X-Linked dominant inheritance (ex)
- PROCESS/Birthmark (ex)
- Synonyms
- Synonym
- Synonym/Bloch-Sulzberger Syndrome
- Synonym/Chromophore nevus/Naegeli
- Synonym/Franceschetti-Jadassohn syndrome
- Synonym/Naegeli incontinentia pigmenti
- Synonym/Naegeli's syndrome/variant
- Laboratory Tests
- Abnormal Lab Findings (Non Measured)
- Chromosomal abnormality (Lab)
- Disease Mechanism & Classification
- Pathophysiology
- Pathophysiology/Chromosomal translocation
- Process
- PROCESS/Chromosomal disorder (ex)
- PROCESS/Congenital/developmental (category)
- PROCESS/Pathophysiologic disorder (category)