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Items: 10

1.

Enuresis, nocturnal, 1

Nocturnal enuresis, or nightly bedwetting in children more than 7 years of age, affects about 10% of 7-year-old children, with a wide range of frequencies between populations. The affliction is often linked to major social maladjustments and occupies considerable time in general medical practice. From the age of 7, there is a spontaneous cure rate of 15% per year, such that few remain affected after the age of 16 years. There are 2 types of nocturnal enuresis: type I, the primary form (PNE), with at least 3 nightly episodes in children older than 7 years, where the child has always had the disorder, and type II, or secondary type, where the child has been dry for at least 6 months but enuresis has recurred (summary by Eiberg et al., 1995). Genetic Heterogeneity of Nocturnal Enuresis ENUR1 has been mapped to chromosome 13q, and ENUR2 has been mapped to chromosome 12q. [from OMIM]

MedGen UID:
124355
Concept ID:
C0270327
Finding; Mental or Behavioral Dysfunction
2.

Enuresis

Lack of the ability to control the urinary bladder leading to involuntary urination at an age where control of the bladder should already be possible. [from HPO]

MedGen UID:
8649
Concept ID:
C0014394
Disease or Syndrome
3.

Primary nocturnal enuresis

MedGen UID:
745677
Concept ID:
C2228139
Finding
4.

Enuresis nocturna

Enuresis occurring during sleeping hours. [from HPO]

MedGen UID:
447309
Concept ID:
CN009503
Finding
5.

Nocturnal

The time in every 24 hour period when it is dark. [from NCI]

MedGen UID:
68706
Concept ID:
C0240526
Temporal Concept
6.

Elimination Disorders

Excretory-related psychiatric disorders usually diagnosed in infancy or childhood. [from MeSH]

MedGen UID:
4911
Concept ID:
C0013895
Mental or Behavioral Dysfunction
7.

Abnormality of the head

An abnormality of the head. [from HPO]

MedGen UID:
867438
Concept ID:
C4021812
Anatomical Abnormality
8.

Macroglossia

MedGen UID:
833250
Concept ID:
CN199633
Finding
9.

Enuresis, nocturnal, 2

MedGen UID:
331473
Concept ID:
C1833268
Disease or Syndrome
10.

Macroglossia

Macroglossia is an abnormal enlargement of the tongue. It is commonly observed with type 2 glycogen storage disease (232300), neurofibromatosis (162200), congenital hypothyroidism, and the Beckwith-Wiedemann syndrome (130650). [from OMIM]

MedGen UID:
3588
Concept ID:
C0009677
Congenital Abnormality
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