Noonan syndrome-like disorder with loose anagen hair

disorder

SNOMED 723444009CUI C1843181

Overview

Noonan syndrome-like disorder with loose anagen hair 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.

Childhood attention deficit/hyperactivity disorder

Always present (100%)HP:0007018

Cognitive delay

Always present (100%)HP:0001263

Increased length of eyelashes

Always present (100%)HP:0000527

Increased width of the forehead

Always present (100%)HP:0000337

Loose anagen hair

Always present (100%)HP:0040169

Loose-jointedness

Always present (100%)HP:0001382

Postnatal failure to thrive

Always present (100%)HP:0001508

Relatively large head

Always present (100%)HP:0004482

Thin, sparse hair

Always present (100%)HP:0008070

Big calvaria

Very frequent (80-99%)HP:0000256

Bulging forehead

Very frequent (80-99%)HP:0011220

Decreased body height

Very frequent (80-99%)HP:0004322

Delayed ability to walk

Very frequent (80-99%)HP:0031936

Generalised decreased muscle tone

Very frequent (80-99%)HP:0001290

Low posterior hair line

Very frequent (80-99%)HP:0002162

Low-set ears

Very frequent (80-99%)HP:0000369

Nasal hypoplasia

Very frequent (80-99%)HP:0003196

Posteriorly angulated ears

Very frequent (80-99%)HP:0000358

Pterygium colli

Very frequent (80-99%)HP:0000465

Retarded ossification

Very frequent (80-99%)HP:0002750

Thinning scalp hair

Very frequent (80-99%)HP:0002209

Atria septal defect

Frequent (30-79%)HP:0001631

Cardiomyopathy, hypertrophic

Frequent (30-79%)HP:0001639

Curly hair

Frequent (30-79%)HP:0002212

Down-slanting palpebral fissure

Frequent (30-79%)HP:0000494

Eczema

Frequent (30-79%)HP:0000964

Epidermal hyperkeratosis

Frequent (30-79%)HP:0000962

Eye drop

Frequent (30-79%)HP:0000508

Feeding difficulties

Frequent (30-79%)HP:0011968

Fetal macrosomia

Frequent (30-79%)HP:0001520

Related Conditions

Autosomal dominant hereditary disorder(parent)

Congenital anomaly of hair(parent)

Multiple malformation syndrome, moderate short stature, facial(parent)

Loose anagen hair syndrome(parent)

Hereditary disorder of the integument(parent)

Congenital anomaly of face(parent)

Developmental hereditary disorder(parent)

Quick Facts

SNOMED CT: 723444009
UMLS CUI: C1843181
Fully Specified Name: Noonan syndrome-like disorder with loose anagen hair (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.