MURCS association

Description

MURCS association, which stands for Müllerian duct aplasia (MU), congenital renal dysplasia (R), cervical somite anomalies (CS), is the atypical (or type II) form of Mayer-Rokitansky-Küster-Hauser syndrome, characterised by utero-vaginal atresia in otherwise normal females as well associated kidney and skeletal abnormalities and hearing problems.

Index terms

MURCS association
Klippel-Feil deformity - conductive deafness - absent vagina
MRKH syndrome type 2

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Mayer-Rokitansky-Küster-Hauser syndrome type 2
Müllerian aplasia - renal aplasia - cervicothoracic somite dysplasia

Exclusions from above levels

http://id.who.int/icd/entity/733825440 – Inborn errors of metabolism

Sibling codes

LD2F.10 – Prune belly syndrome
LD2F.11 – VATER association
LD2F.12 – Sirenomelia
LD2F.13 – Meckel-Gruber syndrome
LD2F.15 – Noonan syndrome
LD2F.16 – Otomandibular dysplasia
LD2F.1Y – Other specified syndromes with multiple structural anomalies, not of environmental origin
LD2F.1Z – Syndromes with multiple structural anomalies, not of environmental origin, unspecified

Foundation entity

MURCS association – http://id.who.int/icd/entity/1521808255

Part of: LD2F.1: Syndromes with multiple structural anomalies, not of environmental origin › LD2F: Syndromes with multiple structural anomalies, without predominant body system involvement › 20: Developmental anomalies