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Patterson syndrome

disorder
SNOMED 771262009CUI C1868546

Overview

Patterson syndrome is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Abnormal limb epiphysis morphology
Very frequent (80-99%)HP:0006505
Abnormal placental size
Very frequent (80-99%)HP:0012767
Abnormality of mandible condylar process
Very frequent (80-99%)HP:3000077
Abnormality of the odontoid process
Very frequent (80-99%)HP:0003310
Acetabular angle flat
Very frequent (80-99%)HP:0003180
Bladder diverticulum
Very frequent (80-99%)HP:0000015
Bronze skin
Very frequent (80-99%)HP:0007574
Deformity of the ethmoid bone
Very frequent (80-99%)HP:0430005
Delayed maturation of pubic bone
Very frequent (80-99%)HP:0008788
Diabetes mellitus
Very frequent (80-99%)HP:0000819
Disproportionately large hands
Very frequent (80-99%)HP:0001176
Furrowed palms and soles
Very frequent (80-99%)HP:0007517
Generalized tonic-clonic seizure (without specification of onset)
Very frequent (80-99%)HP:0002069
Genu valga
Very frequent (80-99%)HP:0002857
Hirsutism
Very frequent (80-99%)HP:0001007
Hyperplasia of nose
Very frequent (80-99%)HP:0000448
Increased bone density in wide portion of long bone
Very frequent (80-99%)HP:0004979
Increased thickness of cranium
Very frequent (80-99%)HP:0002684
Joint swelling
Very frequent (80-99%)HP:0001386
Kyphoscoliosis
Very frequent (80-99%)HP:0002751
Long foot
Very frequent (80-99%)HP:0001833
Macrotia
Very frequent (80-99%)HP:0000400
Mental retardation, severe
Very frequent (80-99%)HP:0010864
Retarded ossification
Very frequent (80-99%)HP:0002750
Upper jaw bone excess
Very frequent (80-99%)HP:0430028
Increased circulating androgen concentration
Frequent (30-79%)HP:0030348
Premature adrenarche
Frequent (30-79%)HP:0012412
Sudden loss of muscle tone
Frequent (30-79%)HP:0010819

Related Conditions

Adrenal hyperfunction(parent)
Small stature(parent)
Congenital pigmentary skin anomalies(parent)
Multiple system malformation syndrome(parent)
Hyperpigmentation of skin(parent)
Genetic intellectual disability(parent)
Genetic disorder of skin pigmentation(parent)

Quick Facts

SNOMED CT
771262009
UMLS CUI
C1868546
Fully Specified Name
Pseudoleprechaunism syndrome Patterson type (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
28
Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.