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Cutis laxa, recessive, type I

disorder
SNOMED 254222002CUI C0268351

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

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

Loose skin
Always present (100%)HP:0000973
Dermatochalasis
Very frequent (80-99%)HP:0010750
Fragmented elastic fibers in the dermis
Very frequent (80-99%)HP:0025167
Lack of skin elasticity
Very frequent (80-99%)HP:0100679
Loose redundant skin
Very frequent (80-99%)HP:0001582
Pulmonary emphysema
Very frequent (80-99%)HP:0002097
Abnormality of cardiovascular system morphology
Frequent (30-79%)HP:0030680
Abnormality of the cheek
Frequent (30-79%)HP:0004426
Abnormality of the face
Frequent (30-79%)HP:0000271
Abnormality of the systemic arterial tree
Frequent (30-79%)HP:0011004
Abnormality of the thoracic cavity
Frequent (30-79%)HP:0045027
Collapsed lung
Frequent (30-79%)HP:0002107
Delayed motor milestones
Frequent (30-79%)HP:0001270
Funny looking face
Frequent (30-79%)HP:0001999
Heart failure
Frequent (30-79%)HP:0001635
Hernia
Frequent (30-79%)HP:0100790
Inguinal hernia
Frequent (30-79%)HP:0000023
Intrauterine growth retardation, IUGR
Frequent (30-79%)HP:0001511
Joint instability
Frequent (30-79%)HP:0001382
Joint subluxation
Frequent (30-79%)HP:0032153
Occlusion of small pulmonary arteries
Frequent (30-79%)HP:0004969
Pathologic fracture
Frequent (30-79%)HP:0002756
Respiratory insufficiency
Frequent (30-79%)HP:0002093
Abnormal cardiac ventricular function
Occasional (5-29%)HP:0030872
Abnormality of the skull bones
Occasional (5-29%)HP:0000929
Aneurysmal disease
Occasional (5-29%)HP:0002617
Dislocated femoral heads
Occasional (5-29%)HP:0002827
Infantile hypertrophic pyloric stenosis
Occasional (5-29%)HP:0002021
Multiple bladder diverticula
Occasional (5-29%)HP:0012619
Pneumonia, recurrent
Occasional (5-29%)HP:0006532

Quick Facts

SNOMED CT
254222002
UMLS CUI
C0268351
Fully Specified Name
Cutis laxa, recessive, type I (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
30
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.