MARCH syndrome

disorder

SNOMED 1169358003CUI C1856053

Overview

MARCH 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.

Arthrogryposis multiplex

Always present (100%)HP:0002804

Brachydactyly

Always present (100%)HP:0001156

Curvature of little finger

Always present (100%)HP:0004209

Cutaneous syndactyly of digits

Always present (100%)HP:0012725

Cystic hygroma of the neck

Always present (100%)HP:0000476

Dysplastic kidneys

Always present (100%)HP:0000110

Fetal foot inversion

Always present (100%)HP:0001762

Hydrancephaly

Always present (100%)HP:0002324

Low-set ears

Always present (100%)HP:0000369

Multinucleated neuron

Always present (100%)HP:4000150

Oligohydramnios

Always present (100%)HP:0001562

Poorly developed lungs

Always present (100%)HP:0002089

Redundant neck skin

Always present (100%)HP:0005989

Retromicrognathia

Always present (100%)HP:0000308

Single flexion crease

Always present (100%)HP:0000954

Small cerebellum

Always present (100%)HP:0001321

Ureteral agenesis

Always present (100%)HP:0012300

Bulbous nasal tip

HP:0000414

Coanal stenosis

HP:0000452

Cystic kidney disease

HP:0000107

Decreased width of nasal dorsum

HP:0000418

Hypoplasia of the brainstem

HP:0002365

Narrow eyelid opening

HP:0045025

Nostrils anteverted

HP:0000463

partial or complete syndactyly 2nd-3rd toes

HP:0004691

Potter facies

HP:0002009

Short neck

HP:0000470

Small kidneys

HP:0000089

Related Conditions

Hydranencephaly(parent)

Developmental hereditary disorder(parent)

Hereditary disorder of nervous system(parent)

Hereditary nephropathy(parent)

Congenital anomaly of the kidney(parent)

Multiple system malformation syndrome(parent)

Recessive hereditary disorder (autosomal)(parent)

Quick Facts

SNOMED CT: 1169358003
UMLS CUI: C1856053
Fully Specified Name: Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, hydranencephaly syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 28

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.