SFMMP (split-foot malformation, mesoaxial polydactyly) syndrome

disorder

SNOMED 1172635005CUI C5567487

Overview

SFMMP (split-foot malformation, mesoaxial polydactyly) 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.

Split hand

Always present (100%)HP:0001171

Bilateral nerve deafness

Very frequent (80-99%)HP:0008619

Foot ectrodactyly

Very frequent (80-99%)HP:0001839

Sensorineural deafness

Very frequent (80-99%)HP:0000407

1-2 toe complete cutaneous syndactyly

Frequent (30-79%)HP:0005767

Absent/small bones of 3rd toe

Frequent (30-79%)HP:0010359

Absent/small outermost 2nd toe bone

Frequent (30-79%)HP:0010413

Absent/small pinky toe bones

Frequent (30-79%)HP:0010383

Absent/underdeveloped bones of 4th toe

Frequent (30-79%)HP:0010371

Aplasia/Hypoplasia of the distal phalanx of the hallux

Frequent (30-79%)HP:0010076

Central polydactyly of feet

Frequent (30-79%)HP:0010112

Nail disease

Frequent (30-79%)HP:0001597

Symphalangism of the proximal phalanx of the 2nd toe with the 2nd metatarsal

Frequent (30-79%)HP:0100483

Webbed 4th-5th toes

Frequent (30-79%)HP:0004692

Webbed first and second toes

Frequent (30-79%)HP:0010711

Central hand polydactyly

HP:0006159

Related Conditions

Sensorineural hearing loss of bilateral ears(parent)

Split foot(parent)

Hearing loss associated with syndrome(parent)

Congenital abnormality of hand and digits(parent)

Congenital anomaly of nail(parent)

Developmental hereditary disorder(parent)

Hereditary disorder of the integument(parent)

Genetic disorder of nail(parent)

Multiple malformation syndrome with limb defect as major feature(parent)

Congenital sensorineural hearing loss(parent)

Recessive hereditary disorder (autosomal)(parent)

Disorder of nail unit of digit of hand(parent)

Hereditary hearing loss(parent)

Quick Facts

SNOMED CT: 1172635005
UMLS CUI: C5567487
Fully Specified Name: Split-foot malformation, mesoaxial polydactyly syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 16

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.