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Brain calcification Rajab type

disorder
SNOMED 720576001CUI C3150910

Overview

Brain calcification Rajab type 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 lung parenchyma morphology
Always present (100%)HP:0006530
Anasarca
Always present (100%)HP:0012050
Birth weight less than 10th percentile
Always present (100%)HP:0001518
Central hypotonia
Always present (100%)HP:0001252
Coughing
Always present (100%)HP:0012735
Decreased amniotic fluid index
Always present (100%)HP:0001562
Decreased body height
Always present (100%)HP:0004322
Decreased size of cranium
Always present (100%)HP:0000252
Deep set eye
Always present (100%)HP:0000490
Deficient in vitamin D
Always present (100%)HP:0100512
Delayed skeletal development
Always present (100%)HP:0002750
Dilatation of the cerebral artery
Always present (100%)HP:0004944
Esophageal varix
Always present (100%)HP:0002040
Fatty liver
Always present (100%)HP:0001397
Feeding difficulties
Always present (100%)HP:0011968
Gastroesophageal reflux disease
Always present (100%)HP:0002020
Growth deficiency
Always present (100%)HP:0001510
Head lag
Always present (100%)HP:0032988
Headache
Always present (100%)HP:0002315
High arched palate
Always present (100%)HP:0000218
Hypoalbuminaemia
Always present (100%)HP:0003073
Inguinal hernia
Always present (100%)HP:0000023
Ligamentous laxity
Always present (100%)HP:0001382
Liver dysfunction, mild
Always present (100%)HP:0001410
Low blood calcium levels
Always present (100%)HP:0002901
Low blood sugar
Always present (100%)HP:0001943
Low levels of vitamin A
Always present (100%)HP:0004905
Low number of red blood cells or haemoglobin
Always present (100%)HP:0001903
Mental and motor retardation
Always present (100%)HP:0001263
Osteopenia
Always present (100%)HP:0000938

Related Conditions

Multiple system malformation syndrome(parent)
Recessive hereditary disorder (autosomal)(parent)
Hereditary degenerative disease of central nervous system(parent)
Calcification of basal ganglia(parent)
Developmental hereditary disorder(parent)
Abnormal cerebral cortex morphology(parent)

Quick Facts

SNOMED CT
720576001
UMLS CUI
C3150910
Fully Specified Name
Brain calcification Rajab type (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.