holoprosencephaly 13, X-linked
MONDO:0026763Mondo
Findings
No curated finding names holoprosencephaly 13, X-linked yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- X-linked recessive inheritance
HPO, annotations 2026-09-02
Features
31 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- MicrocephalyHPOHP:0000252
- 8 of 11 reported patients
- Cleft palateHPOHP:0000175
- 3 of 12 reported patients
- Hearing impairmentHPOHP:0000365
- 3 of 12 reported patients
- Hypoplastic left ventricleHPOHP:0004383
- 3 of 12 reported patients
- MicrognathiaHPOHP:0000347
- 3 of 12 reported patients
- SeizureHPOHP:0001250
- 3 of 12 reported patients
- Thoracic hemivertebraeHPOHP:0008467
- 3 of 12 reported patients
- Ventricular septal defectHPOHP:0001629
- 3 of 12 reported patients
- Alobar holoprosencephalyHPOHP:0006988
- 2 of 12 reported patients
- MicrotiaHPOHP:0008551
- 2 of 12 reported patients
- Semilobar holoprosencephalyHPOHP:0002507
- 2 of 12 reported patients
- Agenesis of corpus callosumHPOHP:0001274
- 1 of 12 reported patients
Show the remaining 19
- Aplasia of the noseHPOHP:0009927
- 1 of 12 reported patients
- Butterfly vertebraeHPOHP:0003316
- 1 of 12 reported patients
- ColpocephalyHPOHP:0030048
- 1 of 12 reported patients
- CyclopiaHPOHP:0009914
- 1 of 12 reported patients
- Double outlet right ventricleHPOHP:0001719
- 1 of 12 reported patients
- Duodenal atresiaHPOHP:0002247
- 1 of 12 reported patients
Where it sits
Other names
1 name
Resolves to: holoprosencephaly 13, X-linked
- Also called
- holoprosencephaly 13, X-linked, X-linked recessive, X-linked dominant