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Disease Comparison Results (show all mode) for Plasminogen activator defect, heredit'y and Say Syndrome 1

Clinical
Demographics
Diseases
Classification
Synonyms
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Found: 70 | Differences: 65

Found: 14 | Differences: 9

Plasminogen activator defect, heredit'y and Say Syndrome 1 sharing 5 common findings. (show all, show common, show differences)

Clinical Manifestations
Signs & Symptoms: Hyperextensable Joints Infant; Particular physiognomy/Odd looking kids; Craniofacial Abnormalities/Congenital; Dermatoglyphic anomalies; Scalp hair sparse/thin; Tongue Protrudes Infant; Delay Sitting Unsupported Infant; Hypotonia; Mouth Hangs Open Infant; Muscles Soft/Doughy Infant; Rolling Over Delay Infant; Tapered fingers; Babkin infant sign/Abnormal; Delayed walking milestone/child; Development Motor Skills (Milestones) Delayed; Galant Infant reflex/Abnormal; Head Neck Floppy Infant Hypotonia Sign; Infant Head Support Delay; Mental Deficiency Child; Moro reflex Poor/Absent Infant; Palmar Grasp infant Reflex Abnormal; Primitive infant reflexes/Abnormal; Rooting infant sign/Abnormal; Swimming infant reflex/Abnormal; Tonic Neck Infant reflex/Abnormal; Shallow Breathing Infant; Hypoplastic distal phalanges; Low set/odd position thumbs; Short tapered thin fingers; Small hands/feet; Growth/development delay; Short stature; Short stature Child; Ptosis (blepharoptosis); Anomalous ears/deformities; Big ears; Prominent Ears
Clinical Presentation & Variations: Presentation/Multiple deformities newborn (odd look)

Demographics & Risk Factors
Population Group: Child; Infant; Population/Pediatrics population
Sex & Age Groups: Population/Children/all; Population/Infant

Associated Diseases & Rule outs
Associated Disease & Complications: Cleft Lip; Cleft lip/deformity; Cleft palate/deformity; Congenital anomalies; Facial dysplasia; Hypospadius anomaly; Mental retardation; Microcephaly/oligophrenia; Micrognathia/congenital small chin; Multiple Congenital Anomalies; Multiple congenital anomalies/Mental retardation; Neonatal Hypotonia/Floppy Baby Syndrome; Renal anomaly/aplasia/hypoplasia; Renal tubular acidosis; Say Syndrome

Disease Mechanism & Classification
Class: CLASS/Jablonski/NIH Archive Anomalies Database; CLASS/Pediatric disorders (ex)
Pathophysiology: Pathophysiology/Maternal Chromosome mutation
Process: PROCESS/Autosomal dominant hereditary disease (ex).; PROCESS/Eponymic (category); PROCESS/Genetic disorder/Spontaneous mutations/sporadic; PROCESS/Hereditofamilial (category); PROCESS/INCIDENCE/Rare disease (ex); PROCESS/Dystostosis/craniofacial (ex)

Synonyms
Synonym: Synonym/Cleft palate-microcephaly-large ears-short stature 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

Disease Mechanism & Classification
Class: CLASS/Pediatric disorders (ex); CLASS/Hematologic (category)
Pathophysiology: Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations); Pathophysiology/Defective fibrinolysis; Pathophysiology/Plasminogen/plasmin cascade disorder
Process: PROCESS/Hereditofamilial (category); PROCESS/Hereditary hypercoagulation/thrombosis disorders (ex)

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