Home
Download
Help
Login
Standard Search
Auto Completion Symptom Search
Advanced Search
Field
Query
Disease
Disease-ID
Orphanet-ID
OMIM-ID
Inheritance
Age of Onset
Comment
Symptom
Pubmed ID
Additional Information
Associated Genes
Internal Classification
Symptoms and Signs
Symptom Definition
Symptom Frequency
Disease Classification
Disease Description/Summary
Diagnosis
Clinical Description
Genotype-Phenotype Correlations
Differential Diagnosis
Management
Genetically Related Disorders
Molecular Genetics
Population Genetics
Field
Term
AND
OR
NOT
Disease
Disease-ID
Orphanet-ID
OMIM-ID
Inheritance
Age of Onset
Comment
Symptom
Pubmed ID
Additional Information
Associated Genes
Internal Classification
Symptoms and Signs
Symptom Definition
Symptom Frequency
Disease Classification
Disease Description/Summary
Diagnosis
Clinical Description
Genotype-Phenotype Correlations
Differential Diagnosis
Management
Genetically Related Disorders
Molecular Genetics
Population Genetics
Field
Term
AND
OR
NOT
Disease
Disease-ID
Orphanet-ID
OMIM-ID
Inheritance
Age of Onset
Comment
Symptom
Pubmed ID
Additional Information
Associated Genes
Internal Classification
Symptoms and Signs
Symptom Definition
Symptom Frequency
Disease Classification
Disease Description/Summary
Diagnosis
Clinical Description
Genotype-Phenotype Correlations
Differential Diagnosis
Management
Genetically Related Disorders
Molecular Genetics
Population Genetics
Field
Term
AND
OR
NOT
Disease
Disease-ID
Orphanet-ID
OMIM-ID
Inheritance
Age of Onset
Comment
Symptom
Pubmed ID
Additional Information
Associated Genes
Internal Classification
Symptoms and Signs
Symptom Definition
Symptom Frequency
Disease Classification
Disease Description/Summary
Diagnosis
Clinical Description
Genotype-Phenotype Correlations
Differential Diagnosis
Management
Genetically Related Disorders
Molecular Genetics
Population Genetics
Field
Term
AND
OR
NOT
Disease
Disease-ID
Orphanet-ID
OMIM-ID
Inheritance
Age of Onset
Comment
Symptom
Pubmed ID
Additional Information
Associated Genes
Internal Classification
Symptoms and Signs
Symptom Definition
Symptom Frequency
Disease Classification
Disease Description/Summary
Diagnosis
Clinical Description
Genotype-Phenotype Correlations
Differential Diagnosis
Management
Genetically Related Disorders
Molecular Genetics
Population Genetics
Field
Term
AND
OR
NOT
Disease
Disease-ID
Orphanet-ID
OMIM-ID
Inheritance
Age of Onset
Comment
Symptom
Pubmed ID
Additional Information
Associated Genes
Internal Classification
Symptoms and Signs
Symptom Definition
Symptom Frequency
Disease Classification
Disease Description/Summary
Diagnosis
Clinical Description
Genotype-Phenotype Correlations
Differential Diagnosis
Management
Genetically Related Disorders
Molecular Genetics
Population Genetics
Symptoms & Signs
Field
Query
Disease
Symptom
Mongolian blue spot
Symptom Information:
Symptom ID:
HPO:0011369
Synonyms:
Mongolian spot [Orphanet:23580]
Mongolian spot (disorder) [Orphanet:23580]
Mongolian Spot [Orphanet:23580]
Mongoloid spot [Orphanet:23580]
Congenital naevus [MedDRA:10067248]
Mongolian spot [MedDRA:10067248]
Congenital nevus [MedDRA:10067248]
Quality:
Cross references:
HPO:0100814 "Blue nevus" [Orphanet:23580]
Orphanet:23580 "Mongoloid spot" [Orphanet:23580]
UMLS:C0265985 "Mongolian Spot" [Orphanet:23580]
Is a (Direct Parents):
MedDRA
Skin neoplasms benign
HPO
Hypermelanotic macule
Orphanet
Abnormality of skin pigmentation
Is a (Whole tree):
HPO:
All(HPO:0000001)
Phenotypic abnormality(HPO:0000118)
Abnormality of the integument(HPO:0001574)
Abnormality of the skin(HPO:0000951)
Generalized abnormality of skin(HPO:0011354)
Abnormality of skin morphology(HPO:0011121)
Abnormality of skin pigmentation(HPO:0001000)
Hyperpigmentation of the skin(HPO:0000953)
Irregular hyperpigmentation(HPO:0007400)
Hypermelanotic macule(HPO:0001034)
Mongolian blue spot(HPO:0011369)
Localized skin lesion(HPO:0011355)
Hypermelanotic macule(HPO:0001034)
Mongolian blue spot(HPO:0011369)
MedDRA:
Skin and subcutaneous tissue disorders(MedDRA:10040785)
Cutaneous neoplasms benign(MedDRA:10040899)
Skin neoplasms benign(MedDRA:10040898)
Mongolian blue spot(HPO:0011369)
Database Frequency:
1 / 7739
Resource:
All diseases associated with this symptom:
Mucopolysaccharidosis type 2
(Orphanet:580)