Schneckenbecken dysplasia

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Schneckenbecken dysplasia

ORPHA:3144Malformation syndrome

Also called Chondrodysplasia with snail-like pelvis · SLC35D1-CDG

What it is

A rare spondylodysplastic dysplasia characterized by the typical radiographic finding of snail-like configuration of the hypoplastic iliac bones. Additional features include flattened hypoplastic vertebral bodies, short ribs, short and wide fibulae, short and broad long bones with a dumbbell-like appearance, and precocious ossification of the tarsus. The malformation is lethal perinatally.

Key facts

Prevalence
<1 / 1 000 000
Age of onset
Antenatal
Inheritance
Autosomal recessive
Classified as
Malformation syndrome

Prevalence figures describe populations, not individuals, and are often estimates from a single study. Where the figure is an incidence or a birth prevalence, it says so.

Signs and symptoms

These ranges are how often a sign appears across everyone diagnosed, not a prediction for one person — most people have some of these and not others. Orphanet also records findings that are specifically absent in this disease; those are in the data but not listed here.

Genes

INPPL1Disease-causing germline mutation(s)
SLC35D1Disease-causing germline mutation(s) (loss of function)

ICD-10 codes

Q77.7filed under a broader ICD-10 category — shared with 47 other rare diseases

ICD-10 has no distinct code for most rare diseases, so many are filed under the nearest available one. A shared code identifies the group, not this disease — the ORPHAcode above is what identifies it.

Related health topics

Reached through the ICD-10 categories this disease is filed under, so these describe the broader group rather than this disease specifically.

Cross-references

GARD 169MESH C536637MONDO 0010013OMIM 269250UMLS C0432194

Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.

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