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German syndrome

disorder
SNOMED 733037000CUI C3887495

Overview

German 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 vocalization
Very frequent (80-99%)HP:0002167
Abnormality of the eyebrow
Very frequent (80-99%)HP:0000534
Arthrogryposis multiplex
Very frequent (80-99%)HP:0002804
Central hypotonia
Very frequent (80-99%)HP:0001252
Concave bridge of nose
Very frequent (80-99%)HP:0005280
Decreased body height
Very frequent (80-99%)HP:0004322
Decreased muscle movement
Very frequent (80-99%)HP:0002375
Deglutition disorder
Very frequent (80-99%)HP:0002015
High forehead
Very frequent (80-99%)HP:0000348
Hypoplastic mandible
Very frequent (80-99%)HP:0000347
Increased width of bridge of nose
Very frequent (80-99%)HP:0000431
Limitation of joint mobility
Very frequent (80-99%)HP:0001376
Narrow head shape
Very frequent (80-99%)HP:0000268
Nonprogressive mental retardation
Very frequent (80-99%)HP:0001249
Onset of lymphedema around puberty
Very frequent (80-99%)HP:0001004
Protruding lower lip
Very frequent (80-99%)HP:0000232
Psychomotor development deficiency
Very frequent (80-99%)HP:0001263
Short and broad skull
Very frequent (80-99%)HP:0000248
Slack jawed appearance
Very frequent (80-99%)HP:0000194
Small midface
Very frequent (80-99%)HP:0011800
Squint
Very frequent (80-99%)HP:0000486
Hearing abnormality
Frequent (30-79%)HP:0000364
High arched palate
Frequent (30-79%)HP:0000218
Oral cleft
Frequent (30-79%)HP:0000202
Proximal interphalangeal finger joint contractures
Frequent (30-79%)HP:0100490
Short neck
Frequent (30-79%)HP:0000470
Unibrow
Frequent (30-79%)HP:0000664
Ambiguous external genitalia
Occasional (5-29%)HP:0000062
Cryptorchidism
Occasional (5-29%)HP:0000028
Down-slanting palpebral fissure
Occasional (5-29%)HP:0000494

Related Conditions

Inherited arthrogryposis(parent)
Multiple malformation syndrome with facial defects as major feature(parent)
Recessive hereditary disorder (autosomal)(parent)
Hereditary lymphedema(parent)

Quick Facts

SNOMED CT
733037000
UMLS CUI
C3887495
Fully Specified Name
German 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.