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
Sparse anterior scalp hair
Symptom Information:
Symptom ID:
HPO:0004768
Synonyms:
Sparse anterior scalp hair [OMIM:Sparse anterior scalp hair]
Quality:
Cross references:
OMIM: "Sparse anterior scalp hair" [OMIM:Sparse anterior scalp hair]
Is a (Direct Parents):
HPO
Abnormality of the frontal hairline
HPO
Sparse scalp hair
Is a (Whole tree):
HPO:
All(HPO:0000001)
Phenotypic abnormality(HPO:0000118)
Abnormality of head or neck(HPO:0000152)
Abnormality of the head(HPO:0000234)
Abnormality of the face(HPO:0000271)
Abnormality of the forehead(HPO:0000290)
Abnormality of the frontal hairline(HPO:0000599)
Sparse anterior scalp hair(HPO:0004768)
Abnormality of the scalp(HPO:0001965)
Abnormality of the scalp hair(HPO:0100037)
Abnormality of the hairline(HPO:0009553)
Abnormality of the frontal hairline(HPO:0000599)
Sparse anterior scalp hair(HPO:0004768)
Sparse scalp hair(HPO:0002209)
Sparse anterior scalp hair(HPO:0004768)
Abnormality of the integument(HPO:0001574)
Abnormality of skin adnexa(HPO:0011138)
Abnormality of the hair(HPO:0001595)
Abnormality of the scalp hair(HPO:0100037)
Abnormality of the hairline(HPO:0009553)
Abnormality of the frontal hairline(HPO:0000599)
Sparse anterior scalp hair(HPO:0004768)
Sparse scalp hair(HPO:0002209)
Sparse anterior scalp hair(HPO:0004768)
Abnormal hair pattern(HPO:0010720)
Congenital abnormal hair pattern(HPO:0011361)
Abnormality of the hairline(HPO:0009553)
Abnormality of the frontal hairline(HPO:0000599)
Sparse anterior scalp hair(HPO:0004768)
Abnormality of hair density(HPO:0011357)
Sparse hair(HPO:0008070)
Sparse scalp hair(HPO:0002209)
Sparse anterior scalp hair(HPO:0004768)
MedDRA:
Database Frequency:
1 / 7739
Resource:
All diseases associated with this symptom:
Tetrasomy 12p
(Orphanet:884)