Piebaldism
- Synonyms
- Piebald skin depigmentation
- Modes of inheritance
- Autosomal dominant inheritance (Orphanet)
Summary
Available tests
Check Related conditions for additional relevant tests.
Clinical tests (44 available)
Clinical features
Help- Abnormality of the digestive system
- Aganglionic megacolon
Aganglionic megacolon
- MedGen UID: 5559
- Concept ID: C0019569
- Finding: Disease or Syndrome
Abnormality of the digestive system
- Aganglionic megacolon
- Abnormality of the eye
- Heterochromia iridis
Heterochromia iridis
- MedGen UID: 98395
- Concept ID: C0423318
- Finding: Finding
Abnormality of the eye
- Heterochromia iridis
- Abnormality of the integument
- Absent pigmentation of the ventral chest
Absent pigmentation of the ventral chest
- MedGen UID: 870403
- Concept ID: C4024848
- Finding: Disease or Syndrome
Abnormality of the integument
- Partial albinism
Partial albinism
- MedGen UID: 1847660
- Concept ID: C5848166
- Finding: Congenital Abnormality
Abnormality of the integument
- Piebaldism
Piebaldism
- MedGen UID: 36361
- Concept ID: C0080024
- Finding: Congenital Abnormality
Abnormality of the integument
- White forelock
White forelock
- MedGen UID: 91023
- Concept ID: C0344312
- Finding: Finding
Abnormality of the integument
- Absent pigmentation of the ventral chest
- Ear malformation
- Ear malformation
Ear malformation
- MedGen UID: 75618
- Concept ID: C0266589
- Finding: Congenital Abnormality
Ear malformation
- Ear malformation
- Neoplasm
- Neoplasm
Neoplasm
- MedGen UID: 10294
- Concept ID: C0027651
- Finding: Neoplastic Process
Neoplasm
- Neoplasm
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