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
Patchy sclerosis of finger phalanx
Symptom Information:
Symptom ID:
HPO:0009772
Synonyms:
Phalangeal sclerosis [HPO:0009772]
Phalangeal sclerosis [OMIM:Phalangeal sclerosis]
Quality:
Cross references:
OMIM: "Phalangeal sclerosis" [OMIM:Phalangeal sclerosis]
Is a (Direct Parents):
HPO
Patchy osteosclerosis
HPO
Sclerosis of finger phalanx
HPO
Patchy sclerosis of hand bones
Is a (Whole tree):
HPO:
All(HPO:0000001)
Phenotypic abnormality(HPO:0000118)
Abnormality of the skeletal system(HPO:0000924)
Abnormality of skeletal morphology(HPO:0011842)
Abnormal appendicular skeleton morphology(HPO:0011844)
Abnormality of limb bone morphology(HPO:0002813)
Abnormality of the upper limb(HPO:0002817)
Abnormality of the hand(HPO:0001155)
Abnormality of finger(HPO:0001167)
Abnormality of phalanx of finger(HPO:0005918)
Sclerosis of finger phalanx(HPO:0100899)
Patchy sclerosis of finger phalanx(HPO:0009772)
Abnormality of digit(HPO:0011297)
Abnormality of finger(HPO:0001167)
Abnormality of phalanx of finger(HPO:0005918)
Sclerosis of finger phalanx(HPO:0100899)
Patchy sclerosis of finger phalanx(HPO:0009772)
Abnormal bone structure(HPO:0003330)
Abnormality of bone mineral density(HPO:0004348)
Patchy changes of bone mineral density(HPO:0010658)
Patchy osteosclerosis(HPO:0005686)
Patchy sclerosis of finger phalanx(HPO:0009772)
Increased bone mineral density(HPO:0011001)
Sclerosis of hand bone(HPO:0004054)
Sclerosis of finger phalanx(HPO:0100899)
Patchy sclerosis of finger phalanx(HPO:0009772)
Irregular sclerosis of hand bones(HPO:0004281)
Patchy sclerosis of hand bones(HPO:0004286)
Patchy sclerosis of finger phalanx(HPO:0009772)
Patchy osteosclerosis(HPO:0005686)
Patchy sclerosis of finger phalanx(HPO:0009772)
MedDRA:
Database Frequency:
1 / 7739
Resource:
All diseases associated with this symptom:
CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE
(OMIM:218400)