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Peters plus syndrome

disorder
SNOMED 449817000CUI C0796012

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.

Broad palm
Always present (100%)HP:0001169
Short hands
Always present (100%)HP:0004279
Anterior chamber synechiae
Very frequent (80-99%)HP:0007833
Bilateral fifth digit clinodactyly
Very frequent (80-99%)HP:0004209
Brachydactyly
Very frequent (80-99%)HP:0001156
Cupid-bow shaped upper lip
Very frequent (80-99%)HP:0002263
Decreased projection of lower jaw
Very frequent (80-99%)HP:0000347
Dull intelligence
Very frequent (80-99%)HP:0001249
Dwarfism, short-limbed
Very frequent (80-99%)HP:0008873
Glaucoma
Very frequent (80-99%)HP:0000501
Hypoplasia of columella
Very frequent (80-99%)HP:0002000
Increased length of philtrum
Very frequent (80-99%)HP:0000343
Mental and motor retardation
Very frequent (80-99%)HP:0001263
Micromelia
Very frequent (80-99%)HP:0002983
Peters anomaly
Very frequent (80-99%)HP:0000659
Round, full face
Very frequent (80-99%)HP:0000311
Scarring or clouding of the cornea of the eye
Very frequent (80-99%)HP:0007957
Short and broad skull
Very frequent (80-99%)HP:0000248
Short neck
Very frequent (80-99%)HP:0000470
Short toes
Very frequent (80-99%)HP:0001831
Small feet
Very frequent (80-99%)HP:0001773
Small for gestational age infant
Very frequent (80-99%)HP:0001511
Vertical enlargement of face
Very frequent (80-99%)HP:0000276
Abnormality of lung artery
Frequent (30-79%)HP:0004414
Abnormality of vision
Frequent (30-79%)HP:0000504
Broad neck
Frequent (30-79%)HP:0000475
Cleft of palate
Frequent (30-79%)HP:0000175
Cleft of upper lip
Frequent (30-79%)HP:0000204
Cornea of eye less than 10mm in diameter
Frequent (30-79%)HP:0000482
Cryptorchidism
Frequent (30-79%)HP:0000028

Related Conditions

Hereditary disorder of the visual system(parent)
Congenital anomaly of anterior chamber of eye(parent)
Recessive hereditary disorder (autosomal)(parent)
Developmental hereditary disorder(parent)

Quick Facts

SNOMED CT
449817000
UMLS CUI
C0796012
Fully Specified Name
Peters plus syndrome (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.