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Items: 7

1.

Inborn genetic diseases

Diseases that are caused by genetic mutations present during embryo or fetal development, although they may be observed later in life. The mutations may be inherited from a parent's genome or they may be acquired in utero. [from HPO]

MedGen UID:
181981
Concept ID:
C0950123
Disease or Syndrome
2.

Metabolic disease

Diseases that are caused by genetic mutations present during embryo or fetal development, although they may be observed later in life. The mutations may be inherited from a parent's genome or they may be acquired in utero. [from HPO]

MedGen UID:
44376
Concept ID:
C0025517
Disease or Syndrome
3.

Disorder of gastrointestinal tract

Diseases that are caused by genetic mutations present during embryo or fetal development, although they may be observed later in life. The mutations may be inherited from a parent's genome or they may be acquired in utero. [from HPO]

MedGen UID:
8970
Concept ID:
C0017178
Disease or Syndrome
4.

Abnormality of the intestine

Diseases that are caused by genetic mutations present during embryo or fetal development, although they may be observed later in life. The mutations may be inherited from a parent's genome or they may be acquired in utero. [from HPO]

MedGen UID:
7130
Concept ID:
C0021831
Disease or Syndrome
5.

Lactose intolerance

Diseases that are caused by genetic mutations present during embryo or fetal development, although they may be observed later in life. The mutations may be inherited from a parent's genome or they may be acquired in utero. [from HPO]

MedGen UID:
6001
Concept ID:
C0022951
Disease or Syndrome
6.

Disorder of digestive system

Diseases that are caused by genetic mutations present during embryo or fetal development, although they may be observed later in life. The mutations may be inherited from a parent's genome or they may be acquired in utero. [from HPO]

MedGen UID:
3828
Concept ID:
C0012242
Disease or Syndrome
7.

Lactose intolerance

Diseases that are caused by genetic mutations present during embryo or fetal development, although they may be observed later in life. The mutations may be inherited from a parent's genome or they may be acquired in utero. [from HPO]

MedGen UID:
505685
Concept ID:
CN004237
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