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Trigonocephaly C syndrome

disorder
SNOMED 715409005CUI C0796095

Overview

Trigonocephaly C 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.

Psychomotor development deficiency
Always present (100%)HP:0001263
Biparietal narrowing
Very frequent (80-99%)HP:0004422
Concave bridge of nose
Very frequent (80-99%)HP:0005280
Cryptorchidism
Very frequent (80-99%)HP:0000028
Decreased projection of mandible
Very frequent (80-99%)HP:0000347
Decreased size of cranium
Very frequent (80-99%)HP:0000252
Female pseudohermaphroditism
Very frequent (80-99%)HP:0010458
Flat philtrum
Very frequent (80-99%)HP:0000319
Gingival hyperplasia
Very frequent (80-99%)HP:0000212
High arched palate
Very frequent (80-99%)HP:0000218
Increased length of philtrum
Very frequent (80-99%)HP:0000343
Low intelligence
Very frequent (80-99%)HP:0001249
Mongoloid slant
Very frequent (80-99%)HP:0000582
Nostrils anteverted
Very frequent (80-99%)HP:0000463
Palpebronasal fold
Very frequent (80-99%)HP:0000286
Permanent curving of the pinkie finger
Very frequent (80-99%)HP:0004209
Posteriorly angulated ears
Very frequent (80-99%)HP:0000358
Short neck
Very frequent (80-99%)HP:0000470
Small nose
Very frequent (80-99%)HP:0003196
Triangular head shape
Very frequent (80-99%)HP:0000243
Underdeveloped ear cartilage
Very frequent (80-99%)HP:0100720
Abnormality of cardiovascular system morphology
Frequent (30-79%)HP:0030680
Abnormality of immune system physiology
Frequent (30-79%)HP:0010978
Abnormality of the anus
Frequent (30-79%)HP:0004378
Bilateral single transverse palmar creases
Frequent (30-79%)HP:0007598
Central hypotonia
Frequent (30-79%)HP:0001252
Decreased body height
Frequent (30-79%)HP:0004322
Decreased volume of lip vermillion
Frequent (30-79%)HP:0000233
Extra oral frenum
Frequent (30-79%)HP:0000191
Failure to thrive in first year of life
Frequent (30-79%)HP:0001531

Related Conditions

Trigonocephaly(parent)
Multiple system malformation syndrome(parent)
Genetic intellectual disability(parent)

Quick Facts

SNOMED CT
715409005
UMLS CUI
C0796095
Fully Specified Name
Trigonocephaly C 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.