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Mohr syndrome

disorder
SNOMED 1779005CUI C0026363

Overview

Mohr 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.

Cleft of palate
Very frequent (80-99%)HP:0000175
Abnormality of lingual frenum
Frequent (30-79%)HP:0000190
Agenesis of central incisor
Frequent (30-79%)HP:0006289
Bifid tip of nose
Frequent (30-79%)HP:0000456
Bilobed tongue
Frequent (30-79%)HP:0010297
Brachydactyly
Frequent (30-79%)HP:0001156
Broad big toe
Frequent (30-79%)HP:0010055
Broad first metatarsal
Frequent (30-79%)HP:0010068
Broad flat nasal bridge
Frequent (30-79%)HP:0000431
Broad, upturned nose
Frequent (30-79%)HP:0000455
Complete duplication of the phalanges of the hallux
Frequent (30-79%)HP:0010100
Concave bridge of nose
Frequent (30-79%)HP:0005280
Decreased body height
Frequent (30-79%)HP:0004322
Deficiency of upper jaw bones
Frequent (30-79%)HP:0000327
Extra oral frenum
Frequent (30-79%)HP:0000191
Finger clinodactyly
Frequent (30-79%)HP:0040019
Hamartoma of tongue
Frequent (30-79%)HP:0011802
High arched palate
Frequent (30-79%)HP:0000218
Hypoplastic teeth
Frequent (30-79%)HP:0000685
Irregular metaphyses
Frequent (30-79%)HP:0003025
Lingual nodules
Frequent (30-79%)HP:0000199
Lobulate tongue
Frequent (30-79%)HP:0000180
Midline cleft lip
Frequent (30-79%)HP:0000161
Partial syndactyly
Frequent (30-79%)HP:0006101
Permanent curving of the pinkie finger
Frequent (30-79%)HP:0004209
Polydactyly affecting the hallux
Frequent (30-79%)HP:0001841
Posterior polydactyly of foot
Frequent (30-79%)HP:0001830
Preaxial hand polydactyly
Frequent (30-79%)HP:0001177
Splayed metaphyses
Frequent (30-79%)HP:0003015
Submucous cleft velum
Frequent (30-79%)HP:0011819

Related Conditions

Oral-facial-digital syndrome(parent)
Developmental hereditary disorder(parent)
Digestive system hereditary disorder(parent)
Hereditary disorder of the integument(parent)
Recessive hereditary disorder (autosomal)(parent)

Quick Facts

SNOMED CT
1779005
UMLS CUI
C0026363
Fully Specified Name
Mohr 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.