Intellectual disability, feeding difficulties, developmental delay, microcephaly syndrome

disorder

SNOMED 773552008CUI C4750955

Overview

Intellectual disability, feeding difficulties, developmental delay, microcephaly 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.

Atria septal defect

Frequent (30-79%)HP:0001631

Autism spectrum disorder

Frequent (30-79%)HP:0000729

Behavioural disorders

Frequent (30-79%)HP:0000708

Birth weight less than 10th percentile

Frequent (30-79%)HP:0001518

Broad bone of big toe

Frequent (30-79%)HP:0010059

Cryptorchidism

Frequent (30-79%)HP:0000028

Curvature of little finger

Frequent (30-79%)HP:0004209

Decreased size of cranium

Frequent (30-79%)HP:0000252

Decreased volume of lip vermillion

Frequent (30-79%)HP:0000233

Decreased volume of upper lip

Frequent (30-79%)HP:0000219

Delayed language development

Frequent (30-79%)HP:0000750

Dilated cerebral ventricle

Frequent (30-79%)HP:0002119

Distortion of face

Frequent (30-79%)HP:0001999

Feeding difficulties

Frequent (30-79%)HP:0011968

Hyperopia

Frequent (30-79%)HP:0000540

Increased length of eyelashes

Frequent (30-79%)HP:0000527

Increased width of permanent maxillary central incisor

Frequent (30-79%)HP:0000675

Neurodevelopmental delay

Frequent (30-79%)HP:0012758

PDA

Frequent (30-79%)HP:0001643

Peripheral hypotonia

Frequent (30-79%)HP:0001252

Poor school performance

Frequent (30-79%)HP:0001249

Poor weight gain

Frequent (30-79%)HP:0001508

Single flexion crease

Frequent (30-79%)HP:0000954

Space between great toe and second toe

Frequent (30-79%)HP:0001852

Squint

Frequent (30-79%)HP:0000486

Susceptibility to infection

Frequent (30-79%)HP:0002719

Thick eyebrow

Frequent (30-79%)HP:0000574

Tooth abnormalities

Frequent (30-79%)HP:0000164

5th finger camptodactyly

Occasional (5-29%)HP:0009183

Abnormal temper tantrums

Occasional (5-29%)HP:0025160

Related Conditions

Multiple malformation syndrome with facial defects as major feature(parent)

Small stature(parent)

Global developmental delay(parent)

Congenital microcephalus(parent)

Genetic intellectual disability(parent)

Quick Facts

SNOMED CT: 773552008
UMLS CUI: C4750955
Fully Specified Name: Intellectual disability, feeding difficulties, developmental delay, microcephaly 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.